Allele Registry

Canonical Allele Identifier: PA104490

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013897

RCV001056948

RCV003887862

ClinVar Variation:

13023

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Asp190Asn	CA256670 NM_000539.3:c.568G>A