Canonical Allele Identifier: PA270024
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 143080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly174Ser
CA270023
NM_000539.3:c.520G>A