Allele Registry

Canonical Allele Identifier: PA104611

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013896

RCV001073422

RCV001857345

ClinVar Variation:

13022

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Gly106Trp	CA256669 NM_000539.3:c.316G>T