Canonical Allele Identifier: PA915977904
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 658930
ClinVar RCV Id: RCV000815853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Pro209Thr
CA5517253
NM_001136178.1:c.625C>A