Allele Registry

Canonical Allele Identifier: PA2826260337

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180874

RCV002515208

ClinVar Variation:

189922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ser1666Phe	CA303314 NM_001202435.3:c.4997C>T