Canonical Allele Identifier: PA126849
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Glu412Lys
CA126847
NM_000399.5:c.1234G>A