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Gene Mutations
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| Records Return:
(3)
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| Gene | Gene Omim Number | Disease Omim Number | Chromosome Location | Gene Mutation | Allelic Variant | Omim Phenotype | Sample Count |
| ENPP1 | 173335 | 208000 | 6q22-q23 | ASN792SER | | ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY | 2 |
| ENPP1 | 173335 | 208000 | 6q22-q23 | PRO305THR | | ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY | 2 |
| ENPP1 | 173335 | 208000 | 6q22-q23 | TYR312TER | | ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY | 2 |
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