Canonical Allele Identifier: PA112183
Gene: CDON HGNC NCBI

Linked Data

ClinVar Variation Id: 30749
ClinVar RCV Id: RCV000023728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230526.1:p.Thr790Ala
CA129438
NM_001243597.2:c.2368A>G