Canonical Allele Identifier: PA2826269034
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1485485
ClinVar RCV Id: RCV002000775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191189.1:p.Gly14Arg
CA361866857
NM_001204260.2:c.40G>C
CA361866858
NM_001204260.2:c.40G>A