Allele Registry

Canonical Allele Identifier: PA915967945

Gene: CCDC88C HGNC NCBI

ClinVar RCV:

RCV000923530

ClinVar Variation:

746885

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073883.2:p.Ala302Val	CA7310060 NM_001080414.4:c.905C>T