Allele Registry

Canonical Allele Identifier: PA2826259086

Gene: SCN1A HGNC NCBI

ClinVar Allele:

187804

ClinVar RCV:

RCV000180816

ClinVar Variation:

189863

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Leu863Trp	CA303139 NM_001202435.3:c.2588T>G