Allele Registry

Canonical Allele Identifier: PA2828471598

Gene: SCN2A HGNC NCBI

ClinVar Allele:

359291

ClinVar RCV:

RCV000414442

RCV002272223

RCV002436235

RCV002509379

ClinVar Variation:

372885

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Arg922His	CA16042346 NM_001371246.1:c.2765G>A