Canonical Allele Identifier: PA314357
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 205357
ClinVar RCV Id: RCV000187314 RCV000541141 RCV003330553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Asp251Asn
CA314356
NM_001909.5:c.751G>A