Canonical Allele Identifier: PA2827938919
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2323038
ClinVar RCV Id: RCV002934119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Pro861Thr
CA358425214
NM_001354819.1:c.2581C>A