Canonical Allele Identifier: PA2826269117
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201944
ClinVar RCV Id: RCV004491289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191190.1:p.Gly11Ala
CA361866818
NM_001204261.2:c.32G>C