Canonical Allele Identifier: PA2826269341
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 760048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191194.1:p.Tyr30His
CA3487139
NM_001204265.2:c.88T>C