Canonical Allele Identifier: PA645481005
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 434873
ClinVar RCV Id: RCV000501059 RCV003335433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003579.3:p.Arg614Cys
CA414195545
NM_003588.4:c.1840C>T