Canonical Allele Identifier: PA1139689459
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 842642
ClinVar RCV Id: RCV001045093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.His420Gln
CA377027234
NM_001136178.1:c.1260C>G
CA377027235
NM_001136178.1:c.1260C>A