Canonical Allele Identifier: PA2826269073
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161495
ClinVar RCV Id: RCV000149029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191189.1:p.Gly326Val
CA174138
NM_001204260.2:c.977G>T