Canonical Allele Identifier: PA2826269035
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201944
ClinVar RCV Id: RCV004491289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191189.1:p.Gly19Ala
CA361866818
NM_001204260.2:c.56G>C