Canonical Allele Identifier: PA915965316
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 664665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Val168Ala
CA342336577
NM_000396.4:c.503T>C