Allele Registry

Canonical Allele Identifier: PA2826260560

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003754165

ClinVar Variation:

2813384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ile1782Val	CA349068080 NM_001202435.3:c.5344A>G