Canonical Allele Identifier: PA915967769
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 465138
ClinVar RCV Id: RCV000532515 RCV001252215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073341.1:p.Gln98His
CA10505718
NM_001079872.2:c.294G>T
CA414205583
NM_001079872.2:c.294G>C