Canonical Allele Identifier: PA1139689200
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 845414
ClinVar RCV Id: RCV001048475 RCV001726424 RCV002372804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Asp237Glu
CA208351706
NM_001136178.1:c.711C>A
CA377029128
NM_001136178.1:c.711C>G