Canonical Allele Identifier: PA915977970
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Arg359Gln
CA343871
NM_001136178.1:c.1076G>A