Allele Registry

Canonical Allele Identifier: PA916036951

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636342

ClinVar Variation:

530466

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Asp888Asn	CA1942691 NM_001353961.2:c.2662G>A