Allele Registry

Canonical Allele Identifier: PA2826014080

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414318

ClinVar Variation:

372740

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Pro1827Leu	CA16042429 NM_001165964.3:c.5480C>T