Allele Registry

Canonical Allele Identifier: PA2828472062

Gene: SCN2A HGNC NCBI

ClinVar Allele:

405352

ClinVar RCV:

RCV000479012

ClinVar Variation:

422520

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Val1215Phe	CA16617268 NM_001371246.1:c.3643G>T