Canonical Allele Identifier: PA2825327829
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201944
ClinVar RCV Id: RCV004491289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018087.1:p.Gly108Ala
CA361866818
NM_001018077.1:c.323G>C