Canonical Allele Identifier: PA314331
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 205344
ClinVar RCV Id: RCV000187300 RCV002516988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ile384Val
CA314330
NM_001909.5:c.1150A>G