Canonical Allele Identifier: PA2499259684
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 1018496
ClinVar RCV Id: RCV001317804
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Gly323Asp
CA5813987
NM_001909.5:c.968G>A