"Mendelics"[submitter] AND "HDAC4"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1684792	NM_001378414.1(HDAC4):c.2863G>C (p.Ala955Pro)	HDAC4 (A950P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 283520	NM_001378414.1(HDAC4):c.2371G>A (p.Ala791Thr)	HDAC4 (A786T +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 801915	NM_001378414.1(HDAC4):c.95-98del	HDAC4	Deletion (intron variant)	not provided +1 more	GBenign

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