Canonical Allele Identifier: PA2826394814
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1699415
ClinVar RCV Id: RCV002273272
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Glu257Lys
CA395479619
NM_001256443.2:c.769G>A