Canonical Allele Identifier: PA645481100
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 434871
ClinVar RCV Id: RCV000502107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003579.3:p.Arg896Gln
CA414192225
NM_003588.4:c.2687G>A