Allele Registry

Canonical Allele Identifier: PA2826013962

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003754165

ClinVar Variation:

2813384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Ile1754Val	CA349068080 NM_001165964.3:c.5260A>G