I am researching the human TP53 gene. Please navigate to the NCBI Gene database, search for 'TP53' in Homo sapiens, and provide the following: the official full name of the gene, the OMIM ID for its primary source, the specific chromosomal location (including the band), one disease explicitly mentioned in its summary, the number of transcript variants and isoforms mentioned due to alternative splicing, and the name of a tool available directly on the page for visualizing genomic data.
Navigate to 'https://www.ncbi.nlm.nih.gov'. Click on the 'Gene' link under 'Popular Resources'. In the search bar, enter 'TP53' and ensure 'Gene' is selected as the database. Click the search button. On the search results page, click on the link for 'TP53 – tumor protein p53' for *Homo sapiens* (human). Locate the 'Summary' section to find the official full name, OMIM ID, and explicitly mentioned disease. Identify the number of transcript variants and isoforms mentioned in the 'Summary' section. Locate the 'Genomic context' section to find the chromosomal location (including the band). Find a tool mentioned on the page for visualizing genomic data. Synthesize all collected information into a concise answer.
The agent successfully navigates to the NCBI Gene database and the specific TP53 gene page for Homo sapiens. The official full name of the gene is stated as 'tumor protein p53'. The OMIM ID for its primary source is stated as '191170'. The specific chromosomal location is stated as '17p13.1'. One disease explicitly mentioned in its summary is stated (e.g., 'human cancers' or 'Li-Fraumeni syndrome'). The number of transcript variants and isoforms mentioned due to alternative splicing is stated as 'multiple'. The name of a tool available directly on the page for visualizing genomic data is stated as 'Genome Data Viewer'.