Canonical Allele Identifier: PA314349
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 205353
ClinVar RCV Id: RCV000231366 RCV000727458 RCV000763725 RCV002372146 RCV003967472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Pro3Leu
CA314348
NM_001909.5:c.8C>T