Allele Registry

Canonical Allele Identifier: PA2827782909

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059405

RCV000723903

RCV001476333

RCV001836728

ClinVar Variation:

68532

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Glu1210Asp	CA234849 NM_001353957.2:c.3630A>C CA349054671 NM_001353957.2:c.3630A>T