Canonical Allele Identifier: PA343873
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Arg359Gln
CA343871
NM_000399.5:c.1076G>A