Allele Registry

Canonical Allele Identifier: PA916036967

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188993

ClinVar Variation:

206859

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Thr907Lys	CA317581 NM_001353961.2:c.2720C>A