Canonical Allele Identifier: PA2580509395
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1946018
ClinVar RCV Id: RCV002667500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Glu15Lys
CA395477050
NM_145239.3:c.43G>A