Canonical Allele Identifier: PA119755
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8571
ClinVar RCV Id: RCV000009102 RCV003555981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Ser701Leu
CA119754
NM_001166104.2:c.2102C>T