Canonical Allele Identifier: PA2826269339
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 351377
ClinVar RCV Id: RCV000317840 RCV002058513 RCV003912497
ClinVar Variation Id: 1333751
ClinVar RCV Id: RCV001808966 RCV003388938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191194.1:p.Arg23Lys
CA3487144
NM_001204265.2:c.68G>A
CA2573052441
NM_001204265.2:c.66_68delinsAAA