Canonical Allele Identifier: PA2826394096
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1443592
ClinVar RCV Id: RCV001955685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Gly26Cys
CA395477177
NM_001256442.2:c.76G>T