Canonical Allele Identifier: PA2826268999
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2309408
ClinVar RCV Id: RCV002870492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191188.1:p.Val422Ala
CA3486847
NM_001204259.2:c.1265T>C