Allele Registry

Canonical Allele Identifier: PA098137

Gene: CTNS HGNC NCBI

ClinVar RCV:

RCV000004710

ClinVar Variation:

4457

HGVS (amino-acid)	Matching Registered Transcripts
NP_004928.2:p.Gly110Val	CA116859 NM_004937.3:c.329G>T