Canonical Allele Identifier: PA314333
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 2194329
ClinVar RCV Id: RCV002637091 RCV002612476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Arg392His
CA314332
NM_001909.5:c.1175G>A