| Approved symbol | RP1L1 |
|---|---|
| Approved name | RP1 like 1 |
| HGCN ID | HGNC:15946 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608581 |
| Chromosome | 8p23.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
