Canonical Allele Identifier: PA2741868087
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2621604
ClinVar RCV Id: RCV003372253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Gly500Arg
CA3100298
NM_001354819.1:c.1498G>A
CA358244716
NM_001354819.1:c.1498G>C