Canonical Allele Identifier: PA658802468
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 522671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Arg193Gln
CA1080488
NM_000396.4:c.578G>A