Canonical Allele Identifier: PA2827938921
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8565
ClinVar RCV Id: RCV000009096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Leu862Pro
CA119742
NM_001354819.1:c.2585T>C