Allele Registry

Canonical Allele Identifier: PA107708

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059461

RCV001390614

RCV002381374

ClinVar Variation:

68585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Gly343Asp	CA285060 NM_001165963.4:c.1028G>A