Canonical Allele Identifier: PA2826269232
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16158
ClinVar RCV Id: RCV000017541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191191.1:p.Phe422Leu
CA126240
NM_001204262.2:c.1264T>C
CA361868666
NM_001204262.2:c.1266C>G
CA361868667
NM_001204262.2:c.1266C>A