Allele Registry

Canonical Allele Identifier: PA2829343557

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV000324537

RCV000353587

RCV001454256

ClinVar Variation:

306429

HGVS (amino-acid)	Matching Registered Transcripts
NP_001805.4:p.Tyr88Cys	CA6220085 NM_001814.6:c.263A>G