Canonical Allele Identifier: PA2827337965
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 434871
ClinVar RCV Id: RCV000502107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317553.1:p.Arg883Gln
CA414192225
NM_001330624.2:c.2648G>A