Canonical Allele Identifier: PA231487
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 130213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Glu459Ala
CA231486
NM_001040142.2:c.1376A>C