Canonical Allele Identifier: PA2573168948
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 1409673
ClinVar RCV Id: RCV001913852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Asp266Tyr
CA342335906
NM_000396.4:c.796G>T