NM_000355.3(TCN2):c.927_930delTCTG (p.Cys309Trpfs) AND Transcobalamin II deficiency ClinVar

NM_000355.3(TCN2):c.776G>C (p.Arg259Pro) AND TCN2 POLYMORPHISM ClinVar

Type: Variation

Species: human

NM_000355.3(TCN2):c.626C>G (p.Ser209Ter) AND Transcobalamin II deficiency ClinVar

Type: Variation

Species: human

NM_000355.3(TCN2):c.427+2T>G AND Transcolabamin II deficiency ClinVar

Type: Variation

Species: human

NM_000355.3(TCN2):c.580+624A>T AND Transcolabamin II deficiency ClinVar

Type: Variation

Species: human

TCN2, 2,152-BP DEL AND 4-BP INS AND Transcolabamin II deficiency ClinVar

Type: Variation

Species: human

Collaborative Study of Genes, Nutrients and Metabolites (CSGNM) dbGaP

ID: phs000789.v1.p1

Description: While many genetic and metabolic studies focus on understanding disease states, this genome wide association study (GWAS) was designed to understand t...

Study Types: Control Set