Canonical Allele Identifier: PA2826268860
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2912076
ClinVar RCV Id: RCV003738722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191187.1:p.Asp38Glu
CA129264896
NM_001204258.1:c.114T>G
CA361867182
NM_001204258.1:c.114T>A