Allele Registry

Canonical Allele Identifier: PA2828472527

Gene: SCN2A HGNC NCBI

ClinVar Variation Id: 2923538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Phe1476Leu	CA349034275 NM_001371246.1:c.4426T>C CA349034303 NM_001371246.1:c.4428C>A CA349034305 NM_001371246.1:c.4428C>G