Canonical Allele Identifier: PA2825158686
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Thr157Ser
CA5517271
NM_000399.5:c.469A>T
CA377030428
NM_000399.5:c.470C>G