Allele Registry

Canonical Allele Identifier: PA2828736338

Gene: CCDC78 HGNC NCBI

ClinVar RCV:

RCV000487557

RCV001851289

RCV002525992

ClinVar Variation:

425081

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364960.1:p.Ala354Asp	CA7789106 NM_001378031.1:c.1061C>A