Canonical Allele Identifier: PA2826018170
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201951
ClinVar RCV Id: RCV004491296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Ser409Pro
CA358246958
NM_001166104.2:c.1225T>C