Canonical Allele Identifier: PA119735
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8559
ClinVar RCV Id: RCV000009090 RCV001804719
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000892.2:p.Leu924Pro
CA119734
NM_000901.5:c.2771T>C