Canonical Allele Identifier: PA2826394797
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468619
ClinVar RCV Id: RCV000543216
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Arg245His
CA7994578
NM_001256443.2:c.734G>A