Canonical Allele Identifier: PA105103
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Val345Met
CA256697
NM_000539.3:c.1033G>A