Allele Registry

Canonical Allele Identifier: PA2827765286

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059486

RCV000519810

ClinVar Variation:

68609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Gly968Arg	CA285111 NM_001353950.2:c.2902G>A CA349060767 NM_001353950.2:c.2902G>C