Canonical Allele Identifier: PA2826018219
Gene: NR3C2 HGNC NCBI
ClinVar RCV:
RCV000009095
ClinVar Variation:
8564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Gly633Arg
CA119740
NM_001166104.2:c.1897G>A
CA358242773
NM_001166104.2:c.1897G>C