Canonical Allele Identifier: PA2827067653
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1684711
ClinVar RCV Id: RCV002247803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307966.1:p.Asp305Gly
CA377027885
NM_001321037.2:c.914A>G