Allele Registry

Canonical Allele Identifier: PA2825356755

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000986861

ClinVar Variation:

801785

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035232.1:p.Leu1563Arg	CA349036509 NM_001040142.2:c.4688T>G