Allele Registry

Canonical Allele Identifier: PA645486907

Gene: CCDC78 HGNC NCBI

ClinVar RCV:

RCV000487557

RCV001851289

RCV002525992

ClinVar Variation:

425081

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026907.2:p.Pro413Thr	CA7789106 NM_001031737.3:c.1237C>A