Canonical Allele Identifier: PA2826268936
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16158
ClinVar RCV Id: RCV000017541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191187.1:p.Phe711Leu
CA126240
NM_001204258.1:c.2131T>C
CA361868666
NM_001204258.1:c.2133C>G
CA361868667
NM_001204258.1:c.2133C>A