Canonical Allele Identifier: PA2499233097
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1039070
ClinVar RCV Id: RCV001342474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Leu172Pro
CA354498744
NM_000539.3:c.515T>C