Allele Registry

Canonical Allele Identifier: PA2826394823

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000024176

RCV002281719

RCV003593864

ClinVar Variation:

31177

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243372.1:p.Arg266Trp	CA259999 NM_001256443.2:c.796C>T