Canonical Allele Identifier: PA658673661
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447313
ClinVar RCV Id: RCV000518023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Arg415His
CA377027272
NM_000399.5:c.1244G>A