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Mutation Direct

Effortless mutation search and display tool

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Gene: CST3 & Disease: ARMD11, 2 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
5635	CST3	c.73G>A	p.Ala25Thr (p.A25T)	NM_000099.4 M	SNV	P	2 +	2
5635	CST3	c.73G>A	p.Ala25Thr (p.A25T)	NM_001288614.2	SNV	P	2 +	2

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