Canonical Allele Identifier: PA2742013148
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2793355
ClinVar RCV Id: RCV003760093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Glu10Val
CA395477021
NM_145239.3:c.29A>T