F13B - Gene browser

F13B

coagulation factor XIII B chain

HCNC Approved Symbol: F13B (HGNC:3534)
Genomic Coordinates: 1:197,038,741 - 197,067,260 (1q31.3)
Synonyms: FXIIIB
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the F13B gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results