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Mutations on the Protein: P07204 From Positions: 460 To 489

3
1
1
1







dbSNP Polymorphism: rs1042579
p.ALA473VAL
N/A
N/A
N/A


Swiss-Prot Disease: VAR_011371
p.ASP486TYR
N/A
N/A
Thrombophilia due to thrombomodulin defect (THPH12)


OMIM Disease: 188040.0001
p.ASP468TYR
N/A
N/A
RECLASSIFIED - VARIANT OF UNKNOWN SIGNIFICANCE






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