Allele Registry

Canonical Allele Identifier: PA2827765137

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059479

RCV000636356

ClinVar Variation:

68602

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Val933Ala	CA285093 NM_001353950.2:c.2798T>C