Canonical Allele Identifier: PA658681079
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 457959
ClinVar RCV Id: RCV000558802 RCV002528310
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Leu7Val
CA379101013
NM_001909.5:c.19C>G