Canonical Allele Identifier: PA2741817886
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 2541724
ClinVar RCV Id: RCV003281999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Gln206Lys
CA30097653
NM_000396.4:c.616C>A