Allele Registry

Canonical Allele Identifier: PA916036968

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059441

ClinVar Variation:

68566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Thr907Arg	CA285009 NM_001353961.2:c.2720C>G