Canonical Allele Identifier: PA2826018163
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 899684
ClinVar RCV Id: RCV001144405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Thr364Ser
CA3100364
NM_001166104.2:c.1090A>T