Allele Registry

Canonical Allele Identifier: PA658676876

Gene: CCDC78 HGNC NCBI

ClinVar RCV:

RCV000516842

RCV000650516

ClinVar Variation:

447011

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026907.2:p.Ala325Pro	CA7789312 NM_001031737.3:c.973G>C