Canonical Allele Identifier: PA916076655
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 808028
ClinVar RCV Id: RCV000996251 RCV001348530 RCV004030204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ala289Val
CA395480201
NM_145239.3:c.866C>T