Canonical Allele Identifier: PA658673639
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452606
ClinVar RCV Id: RCV000761723 RCV001040079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Ala278Thr
CA5517216
NM_000399.5:c.832G>A