Allele Registry

Canonical Allele Identifier: PA2826394763

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000188770

RCV000229187

RCV001535419

RCV002362987

RCV002492869

RCV004537583

ClinVar Variation:

206689

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243372.1:p.Pro216His	CA317031 NM_001256443.2:c.647C>A