Canonical Allele Identifier: PA226284
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98695
ClinVar RCV Id: RCV000085006 RCV000787871 RCV001058357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Pro216Ser
CA226283
NM_000322.5:c.646C>T