Allele Registry

Canonical Allele Identifier: PA098158

Gene: CTNS HGNC NCBI

ClinVar RCV:

RCV000004699

RCV002512764

ClinVar Variation:

4446

HGVS (amino-acid)	Matching Registered Transcripts
NP_004928.2:p.Gly169Asp	CA278065 NM_004937.3:c.506G>A