Canonical Allele Identifier: PA2573173876
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1531238
ClinVar RCV Id: RCV002092369 RCV002473352 RCV003948886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001072.2:p.Arg3612Trp
CA5422277
NM_001081.4:c.10834C>T