Allele Registry

Canonical Allele Identifier: PA2827790643

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001065356

ClinVar Variation:

859283

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Phe1001Ser	CA349067529 NM_001353961.2:c.3002T>C