Canonical Allele Identifier: PA2826394545
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044105
ClinVar RCV Id: RCV001348313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Ser28Cys
CA395477207
NM_001256443.2:c.83C>G