Approved symbol | OPN1SW |
---|---|
Approved name | opsin 1, short wave sensitive |
HGCN ID | HGNC:1012 |
Previous symbols | BCP |
Inheritance | |
OMIM | 613522 |
Chromosome | 7q32.1 |
Panel(s) |
NGS Cone-rod dystrophie en macula degeneratie NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Retinitis pigmentosa NGS Visus pakket Retinale genen |