Canonical Allele Identifier: PA2827067599
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418176
ClinVar Variation Id: 419028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307966.1:p.Ala259dup
CA5517194
NM_001321037.2:c.775_777dup