Allele Registry

Canonical Allele Identifier: PA107877

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059503

RCV000188936

RCV001220193

RCV001786331

ClinVar Variation:

68625

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Leu1309Phe	CA266111 NM_001165963.4:c.3925C>T