| Approved symbol | FSCN2 |
|---|---|
| Approved name | fascin actin-bundling protein 2, retinal |
| HGCN ID | HGNC:3960 |
| Previous symbols | |
| Inheritance | |
| OMIM | 607643 |
| Chromosome | 17q25.3 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
