Allele Registry

Canonical Allele Identifier: PA916036785

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414265

ClinVar Variation:

372903

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Gln613Leu	CA16042437 NM_001353961.2:c.1838A>T