missense mutations
Case#: Patient 69, Spain
DiseaseAssertion: N/A
FamilyInfo: N/A
CasePresentingHPOs: N/A
CaseHPOFreeText: N/A
CaseNotHPOs: N/A
CaseNotHPOFreeText: N/A
CaseEnzymeAssay: N/A
CaseUrineGAGs: N/A
CaseERT: N/A
CaseBMT: N/A
Variant1: c.1205G>A (p.W402X)
Variant1ClinVarID: 11908
Variant1CAID: CA220498
Variant2: c.1187T>C (p.L396P)
Variant2ClinVarID: 4689688
Variant2CAID: CA355963499
AdditionalVariants: N/A
ParentalGenotype: N/A
PreviouslyPublished N/A