Canonical Allele Identifier: PA2825214755
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 932920
ClinVar RCV Id: RCV001200890 RCV002497686
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000892.2:p.Gln391Arg
CA3100347
NM_000901.5:c.1172A>G