Allele Registry

Canonical Allele Identifier: PA107458

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059484

RCV001387943

ClinVar Variation:

68607

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Cys959Arg	CA285105 NM_001165963.4:c.2875T>C