Canonical Allele Identifier: PA2573309971
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 1346867
ClinVar RCV Id: RCV002030225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Gln221Arg
CA88636046
NM_181426.2:c.662A>G