Canonical Allele Identifier: PA144304
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 56342
ClinVar RCV Id: RCV000049755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001072.2:p.Cys225Ser
CA144302
NM_001081.4:c.673T>A
CA376166641
NM_001081.4:c.674G>C