Canonical Allele Identifier: PA119733
Gene: NR3C2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000892.2:p.Ser810Leu
CA119732
NM_000901.5:c.2429C>T