Allele Registry

Canonical Allele Identifier: PA2828475727

Gene: SCN2A HGNC NCBI

ClinVar Allele:

365592

ClinVar RCV:

RCV000440836

ClinVar Variation:

381961

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358176.1:p.Gly1322Arg	CA16603820 NM_001371247.1:c.3964G>A CA349030060 NM_001371247.1:c.3964G>C