Details
| Type | Protein Coding |
| Official Symbol | CYP21A2 |
| Official Name | cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600] |
| Ensembl ID | ENSG00000232414 |
| Bio databases IDs | |
| Aliases | cytochrome P450 family 21 subfamily A member 2 |
| Species | Human, Homo sapiens |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- ADRENAL HYPERPLASIA CONGENITAL DUE TO 21-HYDROXYLASE DEFICIENCY