Allele Registry

Canonical Allele Identifier: PA105119

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013894

RCV001198366

ClinVar Variation:

13020

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Val87Asp	CA256667 NM_000539.3:c.260T>A