Canonical Allele Identifier: PA104268
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Arg381His
CA343874
NM_000399.5:c.1142G>A