Canonical Allele Identifier: PA915977950
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 694853
ClinVar RCV Id: RCV000856960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.His314Pro
CA5517191
NM_001136178.1:c.941A>C