Allele Registry

Canonical Allele Identifier: PA915970227

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV000454700

RCV001512281

RCV001702487

ClinVar Variation:

402572

HGVS (amino-acid)	Matching Registered Transcripts
NP_001805.4:p.Ile153Thr	CA6219956 NM_001814.6:c.458T>C