Canonical Allele Identifier: PA915959316
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 802005
ClinVar RCV Id: RCV000987329

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly106Val
CA354496869
NM_000539.3:c.317G>T