methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria [Source:HGNC Symbol;Acc:25221]
C2orf25, CL25022, cblD
Chromosome 2: 150,443,403-150,444,240 reverse strand.
This transcript has 2 exons, is associated with 502 variant alleles and maps to 70 oligo probes.
This transcript is a product of gene ENSG00000168288.8 Show transcript tableHide transcript table