Canonical Allele Identifier: PA2828132032
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351110.1:p.Arg477His
CA126236
NM_001364181.2:c.1430G>A