Canonical Allele Identifier: PA645492875
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403723
ClinVar RCV Id: RCV000462560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000466.2:p.Gln283Pro
CA16609844
NM_000475.5:c.848A>C
CA2695232187
NM_000475.5:c.848_849delinsCC