Allele Registry

Canonical Allele Identifier: PA317042

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000188775

ClinVar Variation:

206693

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Gly324Ala	CA317041 NM_145239.3:c.971G>C