Allele Registry

Canonical Allele Identifier: PA2827771218

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000493143

RCV001851360

ClinVar Variation:

430089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Asn1367Thr	CA349050334 NM_001353951.2:c.4100A>C