Canonical Allele Identifier: PA915970312
Gene: CTSC HGNC NCBI

Linked Data

ClinVar Variation Id: 7298
ClinVar RCV Id: RCV000007721
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001805.4:p.Trp429Cys
CA118692
NM_001814.6:c.1287G>C
CA382021462
NM_001814.6:c.1287G>T