Canonical Allele Identifier: PA2828131989
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201944
ClinVar RCV Id: RCV004491289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351110.1:p.Gly108Ala
CA361866818
NM_001364181.2:c.323G>C