Canonical Allele Identifier: PA1139735568
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 899686
ClinVar RCV Id: RCV001144407 RCV002482278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Ser312Gly
CA358247844
NM_001354819.1:c.934A>G