Canonical Allele Identifier: PA916078439
Gene: CTSC HGNC NCBI

Linked Data

ClinVar Variation Id: 7296
ClinVar RCV Id: RCV000007719 RCV003764536
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_680475.1:p.Trp39Ser
CA118686
NM_148170.5:c.116G>C