Canonical Allele Identifier: PA2826268938
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16152
ClinVar RCV Id: RCV000017534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191187.1:p.Ile721Met
CA126227
NM_001204258.1:c.2163T>G