Canonical Allele Identifier: PA2826394522
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1929027
ClinVar RCV Id: RCV002618518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Lys12Glu
CA395477032
NM_001256443.2:c.34A>G