GENETIC ENCYCLOPEDIA
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disease: Acquired hemoglobin H disease
id
157
name
Acquired hemoglobin H disease
variant-disease
NM_000489.5(ATRX):c.236C>G (p.Ser79Ter) AND Acquired hemoglobin H disease
NM_000489.5(ATRX):c.20+1G>A AND Acquired hemoglobin H disease
NM_000489.5(ATRX):c.3211G>A (p.Gly1071Arg) AND multiple conditions
NM_000489.5(ATRX):c.7432C>G (p.Pro2478Ala) AND multiple conditions
NM_000489.5(ATRX):c.4070A>G (p.Lys1357Arg) AND multiple conditions
... 3 more