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Mutations on the Protein: NP_937799 From Positions: 120 To 129

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OMIM Disease: 608537.0004
p.ARG126GLY
N/A
N/A
VON HIPPEL-LINDAU SYNDROME


OMIM Disease: 608537.0003
p.ARG126TRP
N/A
N/A
VON HIPPEL-LINDAU SYNDROME||PHEOCHROMOCYTOMA, INCLUDED


OMIM Disease: 608537.0027
p.GLN123ARG
N/A
N/A
VON HIPPEL-LINDAU SYNDROME


OMIM Disease: 608537.0018
p.LEU122PRO
N/A
N/A
RENAL CELL CARCINOMA WITH PARANEOPLASTIC ERYTHROCYTOSIS


OMIM Disease: 608537.0013
p.VAL125PHE
N/A
N/A
VON HIPPEL-LINDAU SYNDROME






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