Allele Registry

Canonical Allele Identifier: PA2827759432

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059405

RCV000723903

RCV001476333

RCV001836728

ClinVar Variation:

68532

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Glu1227Asp	CA234849 NM_001353949.2:c.3681A>C CA349054671 NM_001353949.2:c.3681A>T