Allele Registry

Canonical Allele Identifier: PA105025

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013892

RCV000787682

RCV001002098

RCV001075619

RCV001090660

ClinVar Variation:

13018

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Thr17Met	CA256665 NM_000539.3:c.50C>T