Allele Registry

Canonical Allele Identifier: PA2827768091

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059539

ClinVar Variation:

68659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Ile1771Met	CA285234 NM_001353950.2:c.5313C>G