Allele Registry

Canonical Allele Identifier: PA106887

Gene: CLPP HGNC NCBI

ClinVar RCV:

RCV000049282

RCV002513675

ClinVar Variation:

55868

HGVS (amino-acid)	Matching Registered Transcripts
NP_006003.1:p.Thr145Pro	CA143976 NM_006012.4:c.433A>C