Canonical Allele Identifier: PA2826018122
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2481659
ClinVar RCV Id: RCV003199888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Val48Leu
CA3100504
NM_001166104.2:c.142G>T
CA358250224
NM_001166104.2:c.142G>C