Canonical Allele Identifier: PA645380309
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 344278
ClinVar RCV Id: RCV000322534 RCV002523253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Arg214Cys
CA2716115
NM_181426.2:c.640C>T