Canonical Allele Identifier: PA2825327827
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1485485
ClinVar RCV Id: RCV002000775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018087.1:p.Gly103Arg
CA361866857
NM_001018077.1:c.307G>C
CA361866858
NM_001018077.1:c.307G>A