Canonical Allele Identifier: PA314363
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 205360
ClinVar RCV Id: RCV000864860 RCV001711476 RCV003144152 RCV002314714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Arg309His
CA314362
NM_001909.5:c.926G>A