Canonical Allele Identifier: PA2580260973
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 2195635
ClinVar RCV Id: RCV002628823
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Glu324Lys
CA5813985
NM_001909.5:c.970G>A