Canonical Allele Identifier: PA2825355483
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1521353
ClinVar RCV Id: RCV002031236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Glu1129Gly
CA349022049
NM_001040142.2:c.3386A>G