Canonical Allele Identifier: PA2499231078
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1175283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Cys165Arg
CA364137433
NM_000322.5:c.493T>C