Canonical Allele Identifier: PA645385976
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 282729
ClinVar RCV Id: RCV000308097 RCV000725129 RCV001084655 RCV002429217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ala337Thr
CA5813950
NM_001909.5:c.1009G>A