Canonical Allele Identifier: PA226313
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98709
ClinVar RCV Id: RCV000085022 RCV001705814 RCV002514517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Gly266Asp
CA226312
NM_000322.5:c.797G>A