Allele Registry

Canonical Allele Identifier: PA152209

Gene: CCDC78 HGNC NCBI

ClinVar RCV:

RCV000116603

RCV001516757

RCV001636659

ClinVar Variation:

128631

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026907.2:p.Trp252Arg	CA152208 NM_001031737.3:c.754T>C CA394101022 NM_001031737.3:c.754T>A