Canonical Allele Identifier: PA2825821650
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 916981
ClinVar RCV Id: RCV001173234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129649.1:p.His313Arg
CA377028354
NM_001136177.1:c.938A>G