Canonical Allele Identifier: PA2827337807
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 208797
ClinVar RCV Id: RCV000190825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317553.1:p.Pro37Leu
CA358848
NM_001330624.2:c.110C>T