Allele Registry

Canonical Allele Identifier: PA108692

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059411

RCV000254970

RCV000804975

RCV002326783

ClinVar Variation:

68537

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Val1390Met	CA284940 NM_001165963.4:c.4168G>A