Canonical Allele Identifier: PA2580260940
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 1984385
ClinVar RCV Id: RCV002756799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ala116Val
CA379097960
NM_001909.5:c.347C>T