F8 c.6632C>T ;(p.A2211V)

Variant ID: X-154090084-G-A

NM_000132.3(F8):c.6632C>T;(p.A2211V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiative.

Blood Advances
Johnsen, Jill M JM; Fletcher, Shelley N SN; Huston, Haley H; Roberge, Sarah S; Martin, Beth K BK; Kircher, Martin M; Josephson, Neil C NC; Shendure, Jay J; Ruuska, Sarah S; Koerper, Marion A MA; Morales, Jaime J; Pierce, Glenn F GF; Aschman, Diane J DJ; Konkle, Barbara A BA
Publication Date: 2017-05-23

Variant appearance in text: F8: 6632C>T
PubMed Link: 29296726
Variant Present in the following documents:
  • Main text
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