Canonical Allele Identifier: PA2826018166
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1923297
ClinVar RCV Id: RCV002604522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Ile384Leu
CA3100350
NM_001166104.2:c.1150A>C