Canonical Allele Identifier: PA915977902
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 576866
ClinVar RCV Id: RCV000699471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Ala187Glu
CA377029954
NM_001136178.1:c.560C>A