Canonical Allele Identifier: PA915977943
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Ala278Thr
CA5517216
NM_001136178.1:c.832G>A