Allele Registry

Canonical Allele Identifier: PA2827786032

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188940

RCV001222481

ClinVar Variation:

206818

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Ala1311Asp	CA317429 NM_001353958.2:c.3932C>A