Allele Registry

Canonical Allele Identifier: PA107596

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059404

RCV001344646

ClinVar Variation:

68531

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Gly1233Arg	CA284928 NM_001165963.4:c.3697G>C