Canonical Allele Identifier: PA1139671951
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 984784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Cys185Arg
CA354499200
NM_000539.3:c.553T>C