Allele Registry

Canonical Allele Identifier: PA1139759715

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001067498

ClinVar Variation:

861068

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Val256Met	CA7994584 NM_145239.3:c.766G>A