Canonical Allele Identifier: PA2827337839
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 372872
ClinVar RCV Id: RCV000414616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317553.1:p.Asn146Ser
CA16043210
NM_001330624.2:c.437A>G