Allele Registry

Canonical Allele Identifier: PA658676803

Gene: CCDC78 HGNC NCBI

ClinVar RCV:

RCV000518150

RCV000559318

RCV003915450

ClinVar Variation:

447008

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026907.2:p.Glu128Asp	CA7789632 NM_001031737.3:c.384G>T CA394103638 NM_001031737.3:c.384G>C