Allele Registry

Canonical Allele Identifier: PA2827789861

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001065356

ClinVar Variation:

859283

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Phe1786Ser	CA349067529 NM_001353960.2:c.5357T>C