Canonical Allele Identifier: PA915978002
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Asp383Tyr
CA343133
NM_001136178.1:c.1147G>T