Allele Registry

Canonical Allele Identifier: PA2827755051

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414903

ClinVar Variation:

374394

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Val1784Ala	CA16043651 NM_001353948.2:c.5351T>C