Allele Registry

Canonical Allele Identifier: PA916036758

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000493143

RCV001851360

ClinVar Variation:

430089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Asn564Thr	CA349050334 NM_001353961.2:c.1691A>C