Allele Registry

Canonical Allele Identifier: PA916036744

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000474675

ClinVar Variation:

408922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Cys540Phe	CA16610188 NM_001353961.2:c.1619G>T