Canonical Allele Identifier: PA2580260976
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 2098694
ClinVar RCV Id: RCV003019257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ile338Leu
CA379093257
NM_001909.5:c.1012A>C