Canonical Allele Identifier: PA658681087
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 452273
ClinVar RCV Id: RCV000521394 RCV001853677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Asp45Glu
CA5814283
NM_001909.5:c.135C>G
CA379099811
NM_001909.5:c.135C>A