Canonical Allele Identifier: PA2825359352
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 589603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Met1128Thr
CA59725031
NM_001040143.2:c.3383T>C