Allele Registry

Canonical Allele Identifier: PA645406947

Gene: SCN2A HGNC NCBI

ClinVar Allele:

405340

ClinVar RCV:

RCV000484885

ClinVar Variation:

422127

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Arg102Gln	CA16617256 NM_021007.3:c.305G>A