Allele Registry

Canonical Allele Identifier: PA2828523759

Gene: CTNS HGNC NCBI

ClinVar RCV:

RCV002786022

ClinVar Variation:

1986227

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361424.1:p.Val51Leu	CA397691506 NM_001374495.1:c.151G>C CA397691507 NM_001374495.1:c.151G>T