ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA119733
Gene: NR3C2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
23596
ClinVar RCV:
RCV000009088
ClinVar Variation:
8557
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000892.2:p.Ser810Leu
CA119732
NM_000901.5:c.2429C>T