Canonical Allele Identifier: PA916039478
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8564
ClinVar RCV Id: RCV000009095
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Gly633Arg
CA119740
NM_001354819.1:c.1897G>A
CA358242773
NM_001354819.1:c.1897G>C