F8 c.4925A>G ;(p.E1642G)

Variant ID: X-154157140-T-C

NM_000132.3(F8):c.4925A>G;(p.E1642G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Complexity and diversity of F8 genetic variations in the 1000 genomes.

Journal Of Thrombosis And Haemostasis : Jth
Li, J N JN; Carrero, I G IG; Dong, J F JF; Yu, F L FL
Publication Date: 2015-11

Variant appearance in text: F8: E1642G
PubMed Link: 26383047
Variant Present in the following documents:
  • Main text
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