Canonical Allele Identifier: PA915970267
Gene: CTSC HGNC NCBI

Linked Data

ClinVar Variation Id: 7297
ClinVar RCV Id: RCV000007720 RCV001204386
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001805.4:p.Gly301Ser
CA118689
NM_001814.6:c.901G>A