Allele Registry

Canonical Allele Identifier: PA2827771935

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003754165

ClinVar Variation:

2813384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Ile1771Val	CA349068080 NM_001353951.2:c.5311A>G