Canonical Allele Identifier: PA2825214745
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2588150
ClinVar RCV Id: RCV003344361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000892.2:p.Arg356Trp
CA3100366
NM_000901.5:c.1066C>T