Canonical Allele Identifier: PA2826018251
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8565
ClinVar RCV Id: RCV000009096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Leu862Pro
CA119742
NM_001166104.2:c.2585T>C