Allele Registry

Canonical Allele Identifier: PA2827771939

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414903

ClinVar Variation:

374394

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Val1773Ala	CA16043651 NM_001353951.2:c.5318T>C