Allele Registry

Canonical Allele Identifier: PA2828474000

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000624287

ClinVar Variation:

520403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358176.1:p.Ala263Glu	CA349018097 NM_001371247.1:c.788C>A