Allele Registry

Canonical Allele Identifier: PA2826012711

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000153892

RCV002516100

ClinVar Variation:

167641

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Phe967Cys	CA234856 NM_001165964.3:c.2900T>G