Canonical Allele Identifier: PA2828132047
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16147
ClinVar RCV Id: RCV000017529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351110.1:p.Asp641Val
CA126218
NM_001364181.2:c.1922A>T