Canonical Allele Identifier: PA103513
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 8426
ClinVar RCV Id: RCV000008937 RCV001851751
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Leu309Pro
CA119615
NM_000396.4:c.926T>C