Canonical Allele Identifier: PA2573218143
Gene: CTSC HGNC NCBI

Linked Data

ClinVar Variation Id: 1494465
ClinVar RCV Id: RCV001989362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001805.4:p.Val317Gly
CA382022210
NM_001814.6:c.950T>G