Canonical Allele Identifier: PA645487017
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 286620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Tyr181His
CA10605524
NM_000396.4:c.541T>C