Allele Registry

Canonical Allele Identifier: PA916078439

Gene: CTSC HGNC NCBI

ClinVar Allele:

22335

ClinVar RCV:

RCV000007719

RCV003764536

ClinVar Variation:

7296

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