Allele Registry

Canonical Allele Identifier: PA645392291

Gene: CCDC88C HGNC NCBI

ClinVar RCV:

RCV000442039

RCV004022259

RCV004551417

ClinVar Variation:

376774

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073883.2:p.Arg1299Cys	CA7309192 NM_001080414.4:c.3895C>T