Allele Registry

Canonical Allele Identifier: PA2828471663

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000422689

ClinVar Variation:

390254

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Cys959Arg	CA16604013 NM_001371246.1:c.2875T>C