Allele Registry

Canonical Allele Identifier: PA645407759

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000433186

RCV001265330

RCV002524873

RCV003126721

RCV003985332

ClinVar Variation:

380389

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Arg1635Gln	CA16603923 NM_021007.3:c.4904G>A