Allele Registry

Canonical Allele Identifier: PA2825353695

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000624287

ClinVar Variation:

520403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035232.1:p.Ala263Glu	CA349018097 NM_001040142.2:c.788C>A