Allele Registry

Canonical Allele Identifier: PA2827771996

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001065356

ClinVar Variation:

859283

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Phe1804Ser	CA349067529 NM_001353951.2:c.5411T>C