Canonical Allele Identifier: PA2826394782
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2046903
ClinVar RCV Id: RCV002913967 RCV003427525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.His232Gln
CA395479311
NM_001256443.2:c.696C>A
CA395479312
NM_001256443.2:c.696C>G