Canonical Allele Identifier: PA1139671713
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 984780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly121Ser
CA2607119
NM_000539.3:c.361G>A