Allele Registry

Canonical Allele Identifier: PA2826394816

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001242647

RCV002318094

RCV003595363

ClinVar Variation:

589154

2723191

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243372.1:p.Gly258Arg	CA280410301 NM_001256443.2:c.772G>C CA395479636 NM_001256443.2:c.772G>A