Canonical Allele Identifier: PA916024709
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 430425
ClinVar RCV Id: RCV000493614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307966.1:p.Pro53Leu
CA377031547
NM_001321037.2:c.158C>T