Canonical Allele Identifier: PA103495
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 8421
ClinVar RCV Id: RCV000008932 RCV000623420 RCV001206530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Gly146Arg
CA119608
NM_000396.4:c.436G>C