Canonical Allele Identifier: PA645487008
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 371240
ClinVar RCV Id: RCV000412093
ClinVar Variation Id: 551777
ClinVar RCV Id: RCV000666918 RCV002530701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Met1Ile
CA1080602
NM_000396.4:c.3G>A
CA16040664
NM_000396.4:c.3G>T
CA342337780
NM_000396.4:c.3G>C