Allele Registry

Canonical Allele Identifier: PA2826394327

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001063628

ClinVar Variation:

857864

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243371.1:p.Glu225Ala	CA395479243 NM_001256442.2:c.674A>C