Allele Registry

Canonical Allele Identifier: PA1139671711

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001265183

RCV001265184

ClinVar Variation:

984781

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Gly121Val	CA354497833 NM_000539.3:c.362G>T