Canonical Allele Identifier: PA2826394518
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2793355
ClinVar RCV Id: RCV003760093
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Glu10Val
CA395477021
NM_001256443.2:c.29A>T