Allele Registry

Canonical Allele Identifier: PA106878

Gene: CLPP HGNC NCBI

ClinVar RCV:

RCV000049283

RCV001201399

RCV002513676

ClinVar Variation:

55869

869195

HGVS (amino-acid)	Matching Registered Transcripts
NP_006003.1:p.Cys147Ser	CA143977 NM_006012.4:c.440G>C CA403589616 NM_006012.4:c.439T>A