Allele Registry

Canonical Allele Identifier: PA2825570181

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV001041477

RCV004031252

ClinVar Variation:

839668

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107645.1:p.Leu68Arg	CA225446938 NM_001114173.3:c.203T>G