Canonical Allele Identifier: PA891852047
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 590122
ClinVar RCV Id: RCV002318303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ile390Met
CA379092448
NM_001909.5:c.1170C>G