Canonical Allele Identifier: PA1139742340
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 906592
ClinVar RCV Id: RCV001155878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351114.1:p.Ile498Val
CA361870362
NM_001364185.1:c.1492A>G