Canonical Allele Identifier: PA645492931
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 347728
ClinVar RCV Id: RCV000287250 RCV000882241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000892.2:p.Arg569Gly
CA3100255
NM_000901.5:c.1705A>G