Allele Registry

Canonical Allele Identifier: PA645407662

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000417026

RCV000578327

ClinVar Variation:

375508

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Ala896Val	CA16044307 NM_021007.3:c.2687C>T