Canonical Allele Identifier: PA2826269103
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16158
ClinVar RCV Id: RCV000017541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191189.1:p.Phe648Leu
CA126240
NM_001204260.2:c.1942T>C
CA361868666
NM_001204260.2:c.1944C>G
CA361868667
NM_001204260.2:c.1944C>A