Allele Registry

Canonical Allele Identifier: PA1139759880

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001215553

RCV002511057

ClinVar Variation:

945026

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Gly324Glu	CA395480741 NM_145239.3:c.971G>A