Canonical Allele Identifier: PA2828475932
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3066121
ClinVar RCV Id: RCV003991125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Val1432del
CA2740097952
NM_001371247.1:c.4295_4297del