Allele Registry

Canonical Allele Identifier: PA2828473692

Gene: SCN2A HGNC NCBI

ClinVar Allele:

405340

ClinVar RCV:

RCV000484885

ClinVar Variation:

422127

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358176.1:p.Arg102Gln	CA16617256 NM_001371247.1:c.305G>A