Allele Registry

Canonical Allele Identifier: PA2828471993

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV003797141

ClinVar Variation:

2938319

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Cys1181Phe	CA1940133 NM_001371246.1:c.3542G>T