Canonical Allele Identifier: PA915975419
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 658918
ClinVar RCV Id: RCV000815835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Met326Ile
CA5813956
NM_001909.5:c.978G>A
CA379093400
NM_001909.5:c.978G>T
CA379093403
NM_001909.5:c.978G>C