Allele Registry

Canonical Allele Identifier: PA107725

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059486

RCV000519810

ClinVar Variation:

68609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Gly979Arg	CA285111 NM_001165963.4:c.2935G>A CA349060767 NM_001165963.4:c.2935G>C