Allele Registry

Canonical Allele Identifier: PA171515

Gene: CCDC88C HGNC NCBI

ClinVar RCV:

RCV000145426

RCV000969369

RCV004551273

ClinVar Variation:

158097

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073883.2:p.Asp819Gly	CA171514 NM_001080414.4:c.2456A>G