Canonical Allele Identifier: PA112155
Gene: CDON HGNC NCBI

Linked Data

ClinVar Variation Id: 30747
ClinVar RCV Id: RCV000023726 RCV000419072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230526.1:p.Pro689Ala
CA129434
NM_001243597.2:c.2065C>G