Allele Registry

Canonical Allele Identifier: PA645380408

Gene: CCDC39 HGNC NCBI

ClinVar Variation Id: 242171

HGVS (amino-acid)	Matching Registered Transcripts
NP_852091.1:p.Glu622Gly	CA2715854 NM_181426.2:c.1865A>G