Canonical Allele Identifier: PA2828314081
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 434871
ClinVar RCV Id: RCV000502107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356074.1:p.Arg700Gln
CA414192225
NM_001369145.1:c.2099G>A