Canonical Allele Identifier: PA126235
Gene: NR3C1 HGNC NCBI
ClinVar Allele:
31194
ClinVar RCV:
RCV000017538
ClinVar Variation:
16155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018087.1:p.Leu773Pro
CA126234
NM_001018077.1:c.2318T>C