Canonical Allele Identifier: PA2580137550
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2235663
ClinVar RCV Id: RCV002713250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001072.2:p.Tyr2374His
CA376146440
NM_001081.4:c.7120T>C