Canonical Allele Identifier: PA2580260937
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 1717987
ClinVar RCV Id: RCV002304833
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Pro88Ser
CA379098473
NM_001909.5:c.262C>T