Canonical Allele Identifier: PA2826269031
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 351376
ClinVar RCV Id: RCV000260278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191189.1:p.Val8Met
CA10623094
NM_001204260.2:c.22G>A