Canonical Allele Identifier: PA2580509590
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1699415
ClinVar RCV Id: RCV002273272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Glu257Lys
CA395479619
NM_145239.3:c.769G>A