Allele Registry

Canonical Allele Identifier: PA915970305

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV000007723

ClinVar Variation:

7300

HGVS (amino-acid)	Matching Registered Transcripts
NP_001805.4:p.Tyr412Cys	CA118698 NM_001814.6:c.1235A>G