Canonical Allele Identifier: PA2828471870
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 589603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Met1128Thr
CA59725031
NM_001371246.1:c.3383T>C