Allele Registry

Canonical Allele Identifier: PA2828470731

Gene: SCN2A HGNC NCBI

ClinVar Variation Id: 1342669

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Phe370Leu	CA349020765 NM_001371246.1:c.1108T>C CA349020775 NM_001371246.1:c.1110T>A CA349020777 NM_001371246.1:c.1110T>G