Canonical Allele Identifier: PA915977924
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Ile268Asn
CA126843
NM_001136178.1:c.803T>A