Canonical Allele Identifier: PA2580229427
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1923297
ClinVar RCV Id: RCV002604522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Ile384Leu
CA3100350
NM_001354819.1:c.1150A>C