Canonical Allele Identifier: PA2829343493
Gene: CTSC HGNC NCBI

Linked Data

ClinVar Variation Id: 306433
ClinVar RCV Id: RCV002494957 RCV004021525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001805.4:p.Met1Val