Canonical Allele Identifier: PA2825158669
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1346724
ClinVar RCV Id: RCV002030160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Ala139Ser
CA377030723
NM_000399.5:c.415G>T