Canonical Allele Identifier: PA119756
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8571
ClinVar RCV Id: RCV000009102 RCV003555981
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000892.2:p.Ser818Leu
CA119754
NM_000901.5:c.2453C>T