Canonical Allele Identifier: PA2826055705
Gene: CUL7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1696321
ClinVar RCV Id: RCV002266466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161842.2:p.Met1032Ile
CA364208486
NM_001168370.2:c.3096G>T
CA364208488
NM_001168370.2:c.3096G>C
CA364208489
NM_001168370.2:c.3096G>A