Allele Registry

Canonical Allele Identifier: PA645405185

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414903

ClinVar Variation:

374394

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Val1784Ala	CA16043651 NM_001165963.4:c.5351T>C