DEL17P13.1

Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene.

DEL17P13.1
Identifiers
AliasesC17DELp13.1Chromosome 17p13.1 deletion syndrome
External IDsGeneCards:
Orthologs
SpeciesHumanMouse
Entrez

100653374

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/a
Wikidata
View/Edit Human
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