Canonical Allele Identifier: PA129439
Gene: CDON HGNC NCBI

Linked Data

ClinVar Variation Id: 30749
ClinVar RCV Id: RCV000023728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058648.4:p.Thr790Ala
CA129438
NM_016952.5:c.2368A>G