Allele Registry

Canonical Allele Identifier: PA2828471570

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000118255

RCV000330573

RCV000427650

RCV001083230

RCV002312494

RCV002490810

ClinVar Variation:

130219

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Lys908Arg	CA155058 NM_001371246.1:c.2723A>G