Allele Registry

Canonical Allele Identifier: PA2828473809

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000013735

RCV001048768

RCV002284354

RCV002319419

RCV002513021

ClinVar Variation:

12875

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358176.1:p.Arg188Trp	CA122767 NM_001371247.1:c.562C>T