Allele Registry

Canonical Allele Identifier: PA2741866849

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003754165

ClinVar Variation:

2813384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Ile968Val	CA349068080 NM_001353961.2:c.2902A>G