Canonical Allele Identifier: PA2826018169
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1438837
ClinVar RCV Id: RCV001949083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Asp403Tyr
CA358247019
NM_001166104.2:c.1207G>T