Allele Registry

Canonical Allele Identifier: PA916036973

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000530416

ClinVar Variation:

461280

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Gly911Asp	CA349068786 NM_001353961.2:c.2732G>A