Canonical Allele Identifier: PA645380325
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 344274
ClinVar RCV Id: RCV000270726 RCV001094895 RCV002259338 RCV003972455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Arg294Gly
CA2716064
NM_181426.2:c.880A>G