Canonical Allele Identifier: PA645385968
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 303837
ClinVar RCV Id: RCV000378283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ala314Thr
CA10634247
NM_001909.5:c.940G>A