This spontaneous A-to-G variant at Chr18: 58,035,907 (GRCm38) (T-to-C on negative gene strand) results in the missense mutation p.S2267P in one transcript of fibrillin 2 and p.S998P in a second transcript. (J:211397, J:222308)
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This spontaneous A-to-G variant at Chr18: 58,035,907 (GRCm38) (T-to-C on negative gene strand) results in the missense mutation p.S2267P in one transcript of fibrillin 2 and p.S998P in a second transcript. (J:211397, J:222308)