| Approved symbol | FLVCR1 |
|---|---|
| Approved name | FLVCR heme transporter 1 |
| HGCN ID | HGNC:24682 |
| Previous symbols | AXPC1 |
| Inheritance | |
| OMIM | 609144 |
| Chromosome | 1q32.3 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Movement disorders NGS Neuropathy/Charcot Marie Tooth NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
