C3554127[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2432525	NM_017410.3(HOXC13):c.325C>T (p.Pro109Ser)	HOXC13, HOXC13-AS (P109S)	Single nucleotide variant (missense variant)	Ectodermal dysplasia 9, hair/nail type	GUncertain significance
Select item 2689222	NM_017410.3(HOXC13):c.932G>C (p.Arg311Pro)	HOXC13 (R311P)	Single nucleotide variant (missense variant)	Ectodermal dysplasia 9, hair/nail type	GUncertain significance