Canonical Allele Identifier: PA2828132039
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16151
ClinVar RCV Id: RCV000017533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351110.1:p.Ile559Asn
CA126225
NM_001364181.2:c.1676T>A