Allele Registry

Canonical Allele Identifier: PA3057314241

Gene: CTSC HGNC NCBI

ClinVar RCV:

RCV004801601

ClinVar Variation:

3384330

HGVS (amino-acid)	Matching Registered Transcripts
NP_001805.4:p.His127Arg	CA6219968 NM_001814.6:c.380A>G