Canonical Allele Identifier: PA2825358320
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 130213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Glu459Ala
CA231486
NM_001040143.2:c.1376A>C