Canonical Allele Identifier: PA314343
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 205350
ClinVar RCV Id: RCV000187307 RCV002513999
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Pro88Ala
CA314342
NM_001909.5:c.262C>G