Allele Registry

Canonical Allele Identifier: PA1139759689

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001207813

ClinVar Variation:

938565

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Gly255Glu	CA280410276 NM_145239.3:c.764G>A