Canonical Allele Identifier: PA2826269000
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 736518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191188.1:p.Thr439Ala
CA3486842
NM_001204259.2:c.1315A>G