Canonical Allele Identifier: PA2826268950
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_001191188.1:p.Val12Met
CA10623094
NM_001204259.2:c.34G>A