Canonical Allele Identifier: PA2825821500
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 845414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129649.1:p.Asp237Glu
CA208351706
NM_001136177.1:c.711C>A
CA377029128
NM_001136177.1:c.711C>G