Allele Registry

Canonical Allele Identifier: PA2827771934

Gene: SCN1A HGNC NCBI

ClinVar Allele:

79551

ClinVar RCV:

RCV000059539

ClinVar Variation:

68659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Ile1771Met	CA285234 NM_001353951.2:c.5313C>G