Canonical Allele Identifier: PA2741816699
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 2862844
ClinVar RCV Id: RCV003700030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly329Asp
CA354471173
NM_000539.3:c.986G>A