Canonical Allele Identifier: PA314365
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 205361
ClinVar RCV Id: RCV000187318 RCV001044040
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Pro319Leu
CA314364
NM_001909.5:c.956C>T