Canonical Allele Identifier: PA2826394185
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718129
ClinVar RCV Id: RCV002296581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Glu107Lys
CA395478171
NM_001256442.2:c.319G>A