Allele Registry

Canonical Allele Identifier: PA915970234

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV000007714

RCV000489891

ClinVar Variation:

7291

HGVS (amino-acid)	Matching Registered Transcripts
NP_001805.4:p.Gln252Leu	CA118676 NM_001814.6:c.755A>T