NM_006180.4(NTRK2):c.2165A>G (p.Tyr722Cys) | 4915 | NTRK2 | Pathogenic | 121434633 | RCV000009698; | N | MedGen:C3151303,OMIM:613886 | 9 | 87570425 | 87570425 | NM_006180.4:c.2165A>G | NP_006171.2:p.Tyr722Cys | NC_000009.11:g.87570425A>G | OMIM Allelic Variant:600456.0001 | C3151303 613886 Obesity, hyperphagia, and developmental delay | | |