Canonical Allele Identifier: PA2826394539
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 130039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Glu23Lys
CA231418
NM_001256443.2:c.67G>A