| Approved symbol | P4HA2 |
|---|---|
| Approved name | prolyl 4-hydroxylase subunit alpha 2 |
| HGCN ID | HGNC:8547 |
| Previous symbols | |
| Inheritance | |
| OMIM | 600608 |
| Chromosome | 5q31.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
