Canonical Allele Identifier: PA104733
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13027
ClinVar RCV Id: RCV001074697 RCV000013901
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.His211Pro
CA256674
NM_000539.3:c.632A>C