Allele Registry

Canonical Allele Identifier: PA2826013323

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414265

ClinVar Variation:

372903

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Gln1399Leu	CA16042437 NM_001165964.3:c.4196A>T