Canonical Allele Identifier: PA915977967
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 391755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Glu356Gln
CA16606029
NM_001136178.1:c.1066G>C