VWF c.1173A>G ;(p.T391=)

Variant ID: 12-6174423-T-C

NM_000552.3(VWF):c.1173A>G;(p.T391=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.

The Indian Journal Of Medical Research
Kasatkar, Priyanka P; Ghosh, Kanjaksha K; Shetty, Shrimati S
Publication Date: 2015-12

Variant appearance in text: VWF: T391T
PubMed Link: 26831425
Variant Present in the following documents:
  • Main text
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