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1 protein found in SwissVar (0 variants)

with gene/protein name P61812

Disclaimer: The query results are intended for research purposes only, not for clinical and diagnostic use.

Accession Entry name Disease Variants 3D mapping
(variant position)
P61812 TGFB2_HUMAN family with peters anomaly
P61812 TGFB2_HUMAN loeys-dietz syndrome 4
P61812 TGFB2_HUMAN non-syndromic aortic disease