Canonical Allele Identifier: PA916024712
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 195071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307966.1:p.Pro98Ser
CA241342
NM_001321037.2:c.292C>T