Canonical Allele Identifier: PA645385893
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 284020
ClinVar RCV Id: RCV000326932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ala116Thr
CA5814233
NM_001909.5:c.346G>A