Allele Registry

Canonical Allele Identifier: PA916037007

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059539

ClinVar Variation:

68659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Ile968Met	CA285234 NM_001353961.2:c.2904C>G