Canonical Allele Identifier: PA2825327818
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 760048
ClinVar RCV Id: RCV000937948 RCV001152117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018087.1:p.Tyr30His
CA3487139
NM_001018077.1:c.88T>C