Canonical Allele Identifier: PA645487009
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 371412
ClinVar RCV Id: RCV000409305 RCV003558364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Leu9Pro
CA16040663
NM_000396.4:c.26T>C