Allele Registry

Canonical Allele Identifier: PA1139671931

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001073677

ClinVar Variation:

866002

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Glu181Gln	CA2607204 NM_000539.3:c.541G>C