Canonical Allele Identifier: PA100294
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 17573
ClinVar RCV Id: RCV000019134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Phe229Ile
CA258041
NM_001909.5:c.685T>A