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Mutations on the Protein: P00995 From Positions: 12 To 16

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dbSNP Disease: rs35877720
p.LEU12PHE
N/A
Pancreatitis, hereditary (PCTT)


Swiss-Prot Disease: VAR_011688
p.LEU14PRO
N/A
N/A
Pancreatitis, hereditary (PCTT)


OMIM Disease: 167790.0006
p.LEU14ARG
N/A
N/A
PANCREATITIS, CHRONIC


OMIM Disease: 167790.0005
p.LEU14PRO
N/A
N/A
PANCREATITIS, CHRONIC






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