Canonical Allele Identifier: PA2826269032
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2294739
ClinVar RCV Id: RCV002868227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191189.1:p.Asn11Ser
CA361866875
NM_001204260.2:c.32A>G