Canonical Allele Identifier: PA2826269024
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16149
ClinVar RCV Id: RCV000017531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191188.1:p.Leu668Phe
CA126221
NM_001204259.2:c.2004A>T
CA361868551
NM_001204259.2:c.2004A>C