Allele Registry

Canonical Allele Identifier: PA2826394407

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000188772

ClinVar Variation:

206690

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243371.1:p.Ala291Asp	CA317035 NM_001256442.2:c.872C>A