Canonical Allele Identifier: PA2826268990
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161495
ClinVar RCV Id: RCV000149029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191188.1:p.Gly330Val
CA174138
NM_001204259.2:c.989G>T