Allele Registry

Canonical Allele Identifier: PA100221

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000597212

RCV001206176

RCV001262975

RCV003595384

ClinVar Variation:

499732

2724476

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Gly305Arg	CA7994625 NM_145239.3:c.913G>A CA395480572 NM_145239.3:c.913G>C