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Mutations on the Protein: P69905 From Positions: 99 To 107

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4
0
6




Swiss-Prot Polymorphism: VAR_002820
p.HIS104ARG
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_025390
p.HIS104TYR
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002818
p.LYS100GLU
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002819
p.SER103ARG
N/A
N/A
N/A


OMIM Disease: 141800.0217
p.CYS104SER
N/A
N/A
HEMOGLOBIN OEGSTGEEST


OMIM Disease: 141800.0022
p.HIS103ARG
N/A
N/A
HEMOGLOBIN CONTALDO


OMIM Disease: 141800.0203
p.HIS103TYR
N/A
N/A
HEMOGLOBIN CHAROLLES


OMIM Disease: 141850.0031
p.CYS104TYR
N/A
N/A
HEMOGLOBIN SALLANCHES||HEMOGLOBIN H DISEASE, NONDELETIONAL, INCLUDED


OMIM Disease: 141850.0050
p.HIS103TYR
N/A
N/A
HEMOGLOBIN LOMBARD


OMIM Disease: 141850.0047
p.SER102ARG
N/A
N/A
HEMOGLOBIN MANITOBA






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