Canonical Allele Identifier: PA2827938871
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201951
ClinVar RCV Id: RCV004491296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Ser409Pro
CA358246958
NM_001354819.1:c.1225T>C