Canonical Allele Identifier: PA916004453
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161495
ClinVar RCV Id: RCV000149029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191192.1:p.Gly85Val
CA174138
NM_001204263.2:c.254G>T