Allele Registry

Canonical Allele Identifier: PA2826394461

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001959350

RCV003152784

ClinVar Variation:

1465810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243371.1:p.Gly324Val	CA395480743 NM_001256442.2:c.971G>T