Allele Registry

Canonical Allele Identifier: PA2827782123

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059384

RCV000180909

ClinVar Variation:

68512

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Ser626Gly	CA145235 NM_001353957.2:c.1876A>G