Canonical Allele Identifier: PA174139
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161495
ClinVar RCV Id: RCV000149029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018084.1:p.Gly415Val
CA174138
NM_001018074.1:c.1244G>T