rs200010805

This variant is located in the HPD gene.

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ClinVar annotation

Uncertain Significance★★★☆
3 submitters1 publication

Tyrosinemia type III; Hawkinsinuria; Tyrosinemia type III;Hawkinsinuria; not provided

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About HPD

The protein encoded by this gene is an enzyme in the catabolic pathway of tyrosine. The encoded protein catalyzes the conversion of 4-hydroxyphenylpyruvate to homogentisate. Defects in this gene are a cause of tyrosinemia type 3 (TYRO3) and hawkinsinuria (HAWK). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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