Canonical Allele Identifier: PA658673662
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452607
ClinVar RCV Id: RCV000521478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Ala437Thr
CA377027130
NM_000399.5:c.1309G>A