Canonical Allele Identifier: PA2828132130
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2309408
ClinVar RCV Id: RCV002870492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351111.1:p.Val507Ala
CA3486847
NM_001364182.1:c.1520T>C