Canonical Allele Identifier: PA314319
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 205338
ClinVar RCV Id: RCV000187294 RCV002513998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ala166Val
CA314318
NM_001909.5:c.497C>T