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Mutation Direct

Effortless mutation search and display tool

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Gene: CNPY2 & Disease: FANCC, 2 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
1679340	CNPY2	c.46_50del	p.Gly16fs (p.G16fs)	NM_014255.7 M	Del	LP	2 +	1
1679340	CNPY2	c.46_50del	p.Gly16fs (p.G16fs)	NM_001190991.3	Del	LP	2 +	1

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