Canonical Allele Identifier: PA276037
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 208848
ClinVar RCV Id: RCV000190882
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Gly149Val
CA276036
NM_001909.5:c.446G>T