Allele Registry

Canonical Allele Identifier: PA891859453

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001242647

RCV002318094

RCV003595363

ClinVar Variation:

589154

2723191

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Gly258Arg	CA280410301 NM_145239.3:c.772G>C CA395479636 NM_145239.3:c.772G>A