Canonical Allele Identifier: PA891863610
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 591253
ClinVar RCV Id: RCV000722431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000466.2:p.Ile452Phe
CA412544395
NM_000475.5:c.1354A>T