Allele Registry

Canonical Allele Identifier: PA1139671497

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001265170

RCV001305331

ClinVar Variation:

984772

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Thr17Lys	CA354495380 NM_000539.3:c.50C>A