Allele Registry

Canonical Allele Identifier: PA2828476324

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV001206716

RCV002282481

ClinVar Variation:

937654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358176.1:p.Trp1565Arg	CA349036523 NM_001371247.1:c.4693T>C CA349036526 NM_001371247.1:c.4693T>A