Canonical Allele Identifier: PA2742023738
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 2958764
ClinVar RCV Id: RCV003816987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Cys244Arg
CA2716100
NM_181426.2:c.730T>C