Allele Registry

Canonical Allele Identifier: PA2580509590

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV002273272

ClinVar Variation:

1699415

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Glu257Lys	CA395479619 NM_145239.3:c.769G>A