Canonical Allele Identifier: PA2580509427
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713442
ClinVar RCV Id: RCV002302927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Thr54Ser
CA395477523
NM_145239.3:c.160A>T
CA395477526
NM_145239.3:c.161C>G