Canonical Allele Identifier: PA645496250
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418176
ClinVar Variation Id: 419028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Ala309dup
CA5517194
NM_000399.5:c.925_927dup