Allele Registry

Canonical Allele Identifier: PA1139671704

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001073876

RCV003558653

ClinVar Variation:

866113

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Gly114Val	CA354496965 NM_000539.3:c.341G>T