Allele Registry

Canonical Allele Identifier: PA108758

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059382

ClinVar Variation:

68510

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Val422Glu	CA145232 NM_001165963.4:c.1265T>A