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Mutation Direct

Effortless mutation search and display tool

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Gene: TTR & Disease: MNMN, 2 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
13453	TTR	c.250T>C	p.Phe84Leu (p.F84L)	NM_000371.4 M	SNV	P	3 +	16
246463	TTR	c.122G>A	p.Arg41Gln (p.R41Q)	NM_000371.4 M	SNV	VUS	2 +	6

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