Allele Registry

Canonical Allele Identifier: PA2826394449

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000024170

RCV001067788

ClinVar Variation:

31172

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243371.1:p.Ser317Asn	CA129726 NM_001256442.2:c.950G>A