Canonical Allele Identifier: PA2826269257
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 906592
ClinVar RCV Id: RCV001155878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191192.1:p.Ile167Val
CA361870362
NM_001204263.2:c.499A>G