Canonical Allele Identifier: PA2826394137
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2828907
ClinVar RCV Id: RCV003758221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Gly62Val
CA395477592
NM_001256442.2:c.185G>T