Allele Registry

Canonical Allele Identifier: PA2825359016

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000417026

RCV000578327

ClinVar Variation:

375508

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035233.1:p.Ala896Val	CA16044307 NM_001040143.2:c.2687C>T