Canonical Allele Identifier: PA645383859
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 343274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly51Ala
CA2607070
NM_000539.3:c.152G>C