Canonical Allele Identifier: PA2742013335
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2828783
ClinVar RCV Id: RCV003758219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ala289Asp
CA395480197
NM_145239.3:c.866C>A