Canonical Allele Identifier: PA101148
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16147
ClinVar RCV Id: RCV000017529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000167.1:p.Asp641Val
CA126218
NM_000176.3:c.1922A>T