Allele Registry

Canonical Allele Identifier: PA2826394812

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001304934

ClinVar Variation:

1007709

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243372.1:p.Val256Glu	CA395479614 NM_001256443.2:c.767T>A