Canonical Allele Identifier: PA2580108160
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 1966735
ClinVar RCV Id: RCV002716791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Lys287_Gly288insVal
CA889280469
NM_000396.4:c.862_863insTGG