Allele Registry

Canonical Allele Identifier: PA2580545650

Gene: CCDC39 HGNC NCBI

ClinVar RCV:

RCV002710942

ClinVar Variation:

1963141

HGVS (amino-acid)	Matching Registered Transcripts
NP_852091.1:p.Ser625Asn	CA355308805 NM_181426.2:c.1874G>A