Allele Registry

Canonical Allele Identifier: PA2827789161

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414265

ClinVar Variation:

372903

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Gln1398Leu	CA16042437 NM_001353960.2:c.4193A>T