Allele Registry

Canonical Allele Identifier: PA645380367

Gene: CCDC39 HGNC NCBI

ClinVar Variation Id: 344271

HGVS (amino-acid)	Matching Registered Transcripts
NP_852091.1:p.Gly400Cys	CA2715989 NM_181426.2:c.1198G>T