Allele Registry

Canonical Allele Identifier: PA2826260039

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000986878

ClinVar Variation:

202173

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ile1482Leu	CA275462 NM_001202435.3:c.4444A>C