Allele Registry

Canonical Allele Identifier: PA2826011380

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000189089

RCV001852498

ClinVar Variation:

206942

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Ile68Ser	CA317804 NM_001165964.3:c.203T>G