Canonical Allele Identifier: PA2499232126
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 981507
ClinVar RCV Id: RCV001374469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Phe186Leu
CA342336454
NM_000396.4:c.558C>G
CA342336455
NM_000396.4:c.558C>A
CA342336461
NM_000396.4:c.556T>C