Allele Registry

Canonical Allele Identifier: PA2826013318

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000472521

ClinVar Variation:

408936

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Leu1395Val	CA16610151 NM_001165964.3:c.4183C>G