Allele Registry

Canonical Allele Identifier: PA915970220

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV000007722

RCV002512876

ClinVar Variation:

7299

HGVS (amino-acid)	Matching Registered Transcripts
NP_001805.4:p.His127Pro	CA118695 NM_001814.6:c.380A>C