Allele Registry

Canonical Allele Identifier: PA645407674

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000498653

RCV001283762

RCV002319508

RCV003155947

RCV003766794

ClinVar Variation:

432034

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Arg937His	CA349015776 NM_021007.3:c.2810G>A