Allele Registry

Canonical Allele Identifier: PA1139749660

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV001041477

RCV004031252

ClinVar Variation:

839668

HGVS (amino-acid)	Matching Registered Transcripts
NP_680475.1:p.Leu68Arg	CA225446938 NM_148170.5:c.203T>G