Allele Registry

Canonical Allele Identifier: PA645380367

Gene: CCDC39 HGNC NCBI

ClinVar Allele:

290345

ClinVar RCV:

RCV000404264

RCV000601626

RCV001094814

ClinVar Variation:

344271

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