Canonical Allele Identifier: PA2825460546
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 434871
ClinVar RCV Id: RCV000502107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073341.1:p.Arg878Gln
CA414192225
NM_001079872.2:c.2633G>A