Canonical Allele Identifier: PA2825327887
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1801909
ClinVar RCV Id: RCV002464728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018087.1:p.Met745Val
CA3486687
NM_001018077.1:c.2233A>G