Canonical Allele Identifier: PA314335
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 205346
ClinVar RCV Id: RCV000187302 RCV000632742 RCV002345669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Asn401Ser
CA314334
NM_001909.5:c.1202A>G