Canonical Allele Identifier: PA2741870886
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2912076
ClinVar RCV Id: RCV003738722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351114.1:p.Asp64Glu
CA129264896
NM_001364185.1:c.192T>G
CA361867182
NM_001364185.1:c.192T>A