| Approved symbol | VWA8 |
|---|---|
| Approved name | von Willebrand factor A domain containing 8 |
| HGCN ID | HGNC:29071 |
| Previous symbols | KIAA0564 |
| Inheritance | |
| OMIM | 617509 |
| Chromosome | 13q14.11 |
| Panel(s) |
NGS Cone-rod dystrophie en macula degeneratie NGS Leber congenital amaurosis LCA NGS Retinitis pigmentosa NGS Visus pakket Retinale genen |
