HBB, ASN19LYS
A mutation where the asparargine acid in position 19 in the primary sequence of a beta-chain produced by the HBB gene is replaced by lysine.
Sickle Cell Disease Ontology Project
Term info
curator note
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dc:creator
SCDO (Jade Hotchkiss)
dc:source
http://www.omim.org/entry/141900#0064
existence in other ontologies
Negligable
Beta D-Ouled Rabah Mutation