Allele Registry

Canonical Allele Identifier: PA2826394464

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001215553

RCV002511057

ClinVar Variation:

945026

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243371.1:p.Gly324Glu	CA395480741 NM_001256442.2:c.971G>A