Allele Registry

Canonical Allele Identifier: PA2827758602

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059482

ClinVar Variation:

68605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Trp941Gly	CA285099 NM_001353949.2:c.2821T>G