Canonical Allele Identifier: PA2573218149
Gene: CTSC HGNC NCBI

Linked Data

ClinVar Variation Id: 1420729
ClinVar RCV Id: RCV001943617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001805.4:p.Tyr352Cys
CA6219783
NM_001814.6:c.1055A>G