Abnormal
Case#: No additional case information provided.
DiseaseAssertion: Not specified
FamilyInfo: N/A
CasePresentingHPOs: N/A
CaseHPOFreeText: N/A
CaseNotHPOs: N/A
CaseNotHPOFreeText: N/A
CaseEnzymeAssay: Abnormal
CaseUrineGAGs: Normal
CaseERT: N/A
CaseBMT: N/A
Variant1: c.1504C>T (p.R502W)
Variant1ClinVarID: 2070831
Variant1CAID: CA2802280
Variant2: c.1504C>T (p.R502W)
Variant2ClinVarID: 2070831
Variant2CAID: CA2802280
AdditionalVariants: N/A
ParentalGenotype: N/A
PreviouslyPublished N/A