Allele Registry

Canonical Allele Identifier: PA104701

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013895

RCV001003167

RCV001213959

RCV001813740

ClinVar Variation:

13021

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Gly89Asp	CA256668 NM_000539.3:c.266G>A