Canonical Allele Identifier: PA2828131940
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 906592
ClinVar RCV Id: RCV001155878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351109.1:p.Ile497Val
CA361870362
NM_001364180.2:c.1489A>G