| Approved symbol | OPN1SW |
|---|---|
| Approved name | opsin 1, short wave sensitive |
| HGCN ID | HGNC:1012 |
| Previous symbols | BCP |
| Inheritance | |
| OMIM | 613522 |
| Chromosome | 7q32.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
