Canonical Allele Identifier: PA2580260918
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 2194241
ClinVar RCV Id: RCV002637046
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Pro3Arg
CA379101054
NM_001909.5:c.8C>G