Allele Registry

Canonical Allele Identifier: PA2827776149

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059384

RCV000180909

ClinVar Variation:

68512

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340883.1:p.Ser625Gly	CA145235 NM_001353954.2:c.1873A>G