Allele Registry

Canonical Allele Identifier: PA104713

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013920

RCV001195814

RCV001268622

ClinVar Variation:

13045

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Gly90Asp	CA122823 NM_000539.3:c.269G>A