Allele Registry

Canonical Allele Identifier: PA2825360772

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000189182

RCV003483567

ClinVar Variation:

207029

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035233.1:p.Arg1882Leu	CA318048 NM_001040143.2:c.5645G>T