Canonical Allele Identifier: PA2580260969
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 2110823
ClinVar RCV Id: RCV003042540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Gly303_Val305del
CA2580082672
NM_001909.5:c.908_916del