Canonical Allele Identifier: PA658802228
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 522329
ClinVar RCV Id: RCV000625409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001072.2:p.Ser3491Gly
CA376120540
NM_001081.4:c.10471A>G