Canonical Allele Identifier: PA104296
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Asp383Tyr
CA343133
NM_000399.5:c.1147G>T