Allele Registry

Canonical Allele Identifier: PA107608

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059416

RCV000188935

RCV002514045

ClinVar Variation:

68542

206814

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Gly1433Arg	CA284955 NM_001165963.4:c.4297G>A CA317416 NM_001165963.4:c.4297G>C