Canonical Allele Identifier: PA2499232724
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1205002
ClinVar RCV Id: RCV001571528 RCV002072219 RCV004536203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000466.2:p.Ile470Met
CA10376254
NM_000475.5:c.1410A>G