Canonical Allele Identifier: PA2827938910
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8559
ClinVar RCV Id: RCV000009090 RCV001804719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Leu807Pro
CA119734
NM_001354819.1:c.2420T>C