Allele Registry

Canonical Allele Identifier: PA317111

Gene: SCN1A HGNC NCBI

ClinVar Allele:

201418

ClinVar RCV:

RCV001200251

RCV001318625

ClinVar Variation:

206732

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Ile1955Met	CA317108 NM_001165963.4:c.5865A>G