Canonical Allele Identifier: PA2741818193
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2949366
ClinVar RCV Id: RCV003802092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000466.2:p.Ala170Pro
CA412548613
NM_000475.5:c.508G>C