Canonical Allele Identifier: PA226253
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98677
ClinVar RCV Id: RCV000084985 RCV001250370 RCV002514515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Trp179Arg
CA226252
NM_000322.5:c.535T>C
CA364137344
NM_000322.5:c.535T>A