Allele Registry

Canonical Allele Identifier: PA2827790394

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000153892

RCV002516100

ClinVar Variation:

167641

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Phe181Cys	CA234856 NM_001353961.2:c.542T>G