Canonical Allele Identifier: PA1139718648
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 877668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Lys345Arg
CA379093161
NM_001909.5:c.1034A>G