Canonical Allele Identifier: PA2826394681
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373401
ClinVar RCV Id: RCV000413274 RCV000476515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Pro152His
CA16042942
NM_001256443.2:c.455C>A