Canonical Allele Identifier: PA658811481
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 527781
ClinVar RCV Id: RCV000632767 RCV001821790 RCV002315951 RCV003945587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ser137Leu
CA5814184
NM_001909.5:c.410C>T