Canonical Allele Identifier: PA126228
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16152
ClinVar RCV Id: RCV000017534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018087.1:p.Ile747Met
CA126227
NM_001018077.1:c.2241T>G