Allele Registry

Canonical Allele Identifier: PA2827761298

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059441

ClinVar Variation:

68566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Thr1710Arg	CA285009 NM_001353949.2:c.5129C>G