Canonical Allele Identifier: PA915977871
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 462785
ClinVar RCV Id: RCV000540413 RCV001356784 RCV001108766 RCV002341304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Thr153Pro
CA5517273
NM_001136178.1:c.457A>C