Canonical Allele Identifier: PA2826394080
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1946018
ClinVar RCV Id: RCV002667500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Glu15Lys
CA395477050
NM_001256442.2:c.43G>A