Canonical Allele Identifier: PA913196040
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 626250
ClinVar RCV Id: RCV000768405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Phe175Val
CA364137369
NM_000322.5:c.523T>G