Allele Registry

Canonical Allele Identifier: PA645448625

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000415382

RCV001197506

ClinVar Variation:

374089

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Glu225Gly	CA16043511 NM_145239.3:c.674A>G