Allele Registry

Canonical Allele Identifier: PA2827771645

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000417978

RCV001004732

ClinVar Variation:

381568

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Ile1627Asn	CA16603930 NM_001353951.2:c.4880T>A