Allele Registry

Canonical Allele Identifier: PA094391

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000013739

RCV000810006

RCV001253574

RCV001847597

RCV002274897

RCV002319422

ClinVar Variation:

12879

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035232.1:p.Arg223Gln	CA122772 NM_001040142.2:c.668G>A