Canonical Allele Identifier: PA1139671943
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 867026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gln184Arg
CA354499186
NM_000539.3:c.551A>G