Allele Registry

Canonical Allele Identifier: PA645407704

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000440836

ClinVar Variation:

381961

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Gly1322Arg	CA16603820 NM_021007.3:c.3964G>A CA349030060 NM_021007.3:c.3964G>C