Canonical Allele Identifier: PA2825214763
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2146476
ClinVar RCV Id: RCV003067151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000892.2:p.Ser419Leu
CA3100336
NM_000901.5:c.1256C>T