Canonical Allele Identifier: PA2826268916
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 736518
ClinVar RCV Id: RCV000912175 RCV001155877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191187.1:p.Thr498Ala
CA3486842
NM_001204258.1:c.1492A>G