Allele Registry

Canonical Allele Identifier: PA1139759648

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV001063628

ClinVar Variation:

857864

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Glu225Ala	CA395479243 NM_145239.3:c.674A>C