Allele Registry

Canonical Allele Identifier: PA2826394813

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001067498

ClinVar Variation:

861068

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243372.1:p.Val256Met	CA7994584 NM_001256443.2:c.766G>A