Allele Registry

Canonical Allele Identifier: PA915970312

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV000007721

ClinVar Variation:

7298

HGVS (amino-acid)	Matching Registered Transcripts
NP_001805.4:p.Trp429Cys	CA118692 NM_001814.6:c.1287G>C CA382021462 NM_001814.6:c.1287G>T