Allele Registry

Canonical Allele Identifier: PA645380494

Gene: CCDC39 HGNC NCBI

ClinVar Variation Id: 228476

HGVS (amino-acid)	Matching Registered Transcripts
NP_852091.1:p.Arg853Cys	CA2715643 NM_181426.2:c.2557C>T