Canonical Allele Identifier: PA103484
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 8423
ClinVar RCV Id: RCV000008934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Ala277Val
CA119611
NM_000396.4:c.830C>T
CA2499214164
NM_000396.4:c.830_831delinsTG