Canonical Allele Identifier: PA916078434
Gene: CTSC HGNC NCBI

Linked Data

ClinVar Variation Id: 306433
ClinVar RCV Id: RCV002494957 RCV004021525
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_680475.1:p.Met1Val