Canonical Allele Identifier: PA2741868086
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2789164
ClinVar RCV Id: RCV003674552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Ser415Arg
CA358246850
NM_001354819.1:c.1245C>G
CA358246852
NM_001354819.1:c.1245C>A
CA358246865
NM_001354819.1:c.1243A>C