Allele Registry

Canonical Allele Identifier: PA2741866861

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003752662

ClinVar Variation:

2864086

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Trp998Leu	CA349067586 NM_001353961.2:c.2993G>T