Canonical Allele Identifier: PA915955241
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 695689
ClinVar RCV Id: RCV000861550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001072.2:p.Ser2371Phe
CA5423454
NM_001081.4:c.7112C>T