Allele Registry

Canonical Allele Identifier: PA916036941

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000441570

RCV002522649

ClinVar Variation:

391762

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Ala871Ser	CA1942700 NM_001353961.2:c.2611G>T