Canonical Allele Identifier: PA2573218114
Gene: CTSC HGNC NCBI

Linked Data

ClinVar Variation Id: 1679189
ClinVar RCV Id: RCV002226632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001805.4:p.Thr121dup
CA2573147795
NM_001814.6:c.360_362dup