Canonical Allele Identifier: PA2827067630
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 952751
ClinVar RCV Id: RCV001224920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307966.1:p.Arg268Pro
CA377028294
NM_001321037.2:c.803G>C