Canonical Allele Identifier: PA916044696
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16158
ClinVar RCV Id: RCV000017541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351114.1:p.Phe738Leu
CA126240
NM_001364185.1:c.2212T>C
CA361868666
NM_001364185.1:c.2214C>G
CA361868667
NM_001364185.1:c.2214C>A