Allele Registry

Canonical Allele Identifier: PA2827788055

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV002314381

ClinVar Variation:

588285

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Ser625Cys	CA349067383 NM_001353960.2:c.1873A>T