Allele Registry

Canonical Allele Identifier: PA2826394773

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001359644

ClinVar Variation:

1051581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243372.1:p.Val223Ile	CA395479218 NM_001256443.2:c.667G>A