Allele Registry

Canonical Allele Identifier: PA202102

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000176763

RCV000189181

RCV000417008

RCV001265414

RCV001847815

RCV001849328

RCV002516714

ClinVar Variation:

196039

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Arg1882Gln	CA202100 NM_021007.3:c.5645G>A