Canonical Allele Identifier: PA2573309973
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 1405756
ClinVar RCV Id: RCV001935249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Ile224Val
CA2716107
NM_181426.2:c.670A>G