Canonical Allele Identifier: PA645487012
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 292587
ClinVar RCV Id: RCV000390371 RCV000892785 RCV003165783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Ile57Val
CA1080562
NM_000396.4:c.169A>G