Allele Registry

Canonical Allele Identifier: PA915970252

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV000661991

RCV001332042

RCV003767920

ClinVar Variation:

548504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001805.4:p.Arg272Pro	CA6219835 NM_001814.6:c.815G>C