Allele Registry

Canonical Allele Identifier: PA317036

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000188772

ClinVar Variation:

206690

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Ala291Asp	CA317035 NM_145239.3:c.872C>A