Allele Registry

Canonical Allele Identifier: PA2741830616

Gene: CCDC88C HGNC NCBI

ClinVar RCV:

RCV003356861

ClinVar Variation:

2600548

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073883.2:p.Ala303Ser	CA7310058 NM_001080414.4:c.907G>T