Canonical Allele Identifier: PA2826018250
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2903639
ClinVar RCV Id: RCV003726828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Pro861Leu
CA358425209
NM_001166104.2:c.2582C>T