Allele Registry

Canonical Allele Identifier: PA916036411

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000413718

ClinVar Variation:

372972

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Leu869Ser	CA16042442 NM_001353948.2:c.2606T>C