Canonical Allele Identifier: PA2826269302
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191193.1:p.Arg142His
CA126236
NM_001204264.2:c.425G>A