Canonical Allele Identifier: PA2741890667
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 2507189
ClinVar RCV Id: RCV003239080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Pro89Leu
CA379098457
NM_001909.5:c.266C>T