| Approved symbol | RP2 |
|---|---|
| Approved name | RP2 activator of ARL3 GTPase |
| HGCN ID | HGNC:10274 |
| Previous symbols | |
| Inheritance | |
| OMIM | 300757 |
| Chromosome | Xp11.3 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB RP2 Analysis |
