Canonical Allele Identifier: PA2828132151
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16158
ClinVar RCV Id: RCV000017541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351111.1:p.Phe737Leu
CA126240
NM_001364182.1:c.2209T>C
CA361868666
NM_001364182.1:c.2211C>G
CA361868667
NM_001364182.1:c.2211C>A