Canonical Allele Identifier: PA100310
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 17574
ClinVar RCV Id: RCV000019135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Trp383Cys
CA258042
NM_001909.5:c.1149G>C
CA379092527
NM_001909.5:c.1149G>T