Allele Registry

Canonical Allele Identifier: PA2828472331

Gene: SCN2A HGNC NCBI

ClinVar Allele:

362320

ClinVar RCV:

RCV000417028

ClinVar Variation:

375509

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Cys1344Tyr	CA16044309 NM_001371246.1:c.4031G>A