Allele Registry

Canonical Allele Identifier: PA2826013966

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414903

ClinVar Variation:

374394

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Val1756Ala	CA16043651 NM_001165964.3:c.5267T>C