Allele Registry

Canonical Allele Identifier: PA2825359747

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000436036

ClinVar Variation:

391368

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035233.1:p.Ala1329Ser	CA16603921 NM_001040143.2:c.3985G>T