Canonical Allele Identifier: PA103503
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 8424
ClinVar RCV Id: RCV000008935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Gly79Glu
CA119612
NM_000396.4:c.236G>A