Canonical Allele Identifier: PA1139689278
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418176
ClinVar Variation Id: 419028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Ala309dup
CA5517194
NM_001136178.1:c.925_927dup