Allele Registry

Canonical Allele Identifier: PA2827770920

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059494

ClinVar Variation:

68617

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Thr1199Lys	CA285129 NM_001353951.2:c.3596C>A