VWF c.665G>T ;(p.W222L)

Variant ID: 12-6184710-C-A

NM_000552.3(VWF):c.665G>T;(p.W222L)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Genetic analysis of carrier status in female members of Japanese hemophilia families.

Journal Of Thrombosis And Haemostasis : Jth
Shinozawa, Keiko K; Amano, Kagehiro K; Hagiwara, Takeshi T; Bingo, Masato M; Chikasawa, Yushi Y; Inaba, Hiroshi H; Kinai, Ei E; Fukutake, Katsuyuki K
Publication Date: 2021-06

Variant appearance in text: VWF: Trp222Leu
PubMed Link: 33760382
Variant Present in the following documents:
  • Main text
  • JTH-19-1493.pdf
View BVdb publication page