Canonical Allele Identifier: PA2825460304
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_001073341.1:p.Pro32Leu
CA358848
NM_001079872.2:c.95C>T