Allele Registry

Canonical Allele Identifier: PA278468

Gene: CTNS HGNC NCBI

ClinVar RCV:

RCV000169014

RCV000258027

RCV002516526

ClinVar Variation:

188718

HGVS (amino-acid)	Matching Registered Transcripts
NP_004928.2:p.Asp205del	CA278466 NM_004937.3:c.614_616del