Canonical Allele Identifier: PA891851990
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 568472
ClinVar RCV Id: RCV000688842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ile85Val
CA379098522
NM_001909.5:c.253A>G