Canonical Allele Identifier: PA358849
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 208797
ClinVar RCV Id: RCV000190825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003579.3:p.Pro50Leu
CA358848
NM_003588.4:c.149C>T