Canonical Allele Identifier: PA2826394661
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 206683
ClinVar RCV Id: RCV000188762 RCV002228827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Ala139Thr
CA317019
NM_001256443.2:c.415G>A