Allele Registry

Canonical Allele Identifier: PA2825355625

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000551875

RCV001556515

RCV002265794

RCV002456120

ClinVar Variation:

464907

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035232.1:p.Arg1177Trp	CA1940130 NM_001040142.2:c.3529C>T