Canonical Allele Identifier: PA2826394852
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 847965
ClinVar RCV Id: RCV001051614
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Ala289Thr
CA7994591
NM_001256443.2:c.865G>A