Canonical Allele Identifier: PA226294
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98699
ClinVar RCV Id: RCV000085011 RCV001075618 RCV001003141 RCV001346727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Arg220Gln
CA226293
NM_000322.5:c.659G>A