| Approved symbol | KCNV2 |
|---|---|
| Approved name | potassium voltage-gated channel modifier subfamily V member 2 |
| HGCN ID | HGNC:19698 |
| Previous symbols | |
| Inheritance | |
| OMIM | 607604 |
| Chromosome | 9p24.2 |
| Panel(s) |
NGS Cone-rod dystrophie en macula degeneratie NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Retinitis pigmentosa NGS Visus pakket Retinale genen |
