Allele Registry

Canonical Allele Identifier: PA2827783027

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000483132

ClinVar Variation:

421599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Lys1285Thr	CA16617296 NM_001353957.2:c.3854A>C