Allele Registry

Canonical Allele Identifier: PA916036999

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000471658

ClinVar Variation:

408934

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Ser959Tyr	CA16610233 NM_001353961.2:c.2876C>A