Allele Registry

Canonical Allele Identifier: PA2827765768

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000587683

RCV002530921

ClinVar Variation:

496119

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Val1157Ile	CA1942940 NM_001353950.2:c.3469G>A