Canonical Allele Identifier: PA2580260972
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 2071655
ClinVar RCV Id: RCV002975750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Val318Met
CA5813992
NM_001909.5:c.952G>A