Canonical Allele Identifier: PA645487024
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 370960
ClinVar RCV Id: RCV000409981
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Arg312Gly
CA1080390
NM_000396.4:c.934C>G