Canonical Allele Identifier: PA2826394853
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 808028
ClinVar RCV Id: RCV000996251 RCV001348530 RCV004030204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Ala289Val
CA395480201
NM_001256443.2:c.866C>T