VWF c.1378C>T ;(p.H460Y)

Variant ID: 12-6173466-G-A

NM_000552.3(VWF):c.1378C>T;(p.H460Y)

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:

Application of high-throughput sequencing for hereditary thrombocytopenia in southwestern China.

Journal Of Clinical Laboratory Analysis
Zhang, Luying L; Yu, Jie J; Xian, Ying Y; Wen, Xianhao X; Guan, Xianmin X; Guo, Yuxia Y; Luo, Mingzhu M; Dou, Ying Y
Publication Date: 2021-08

Variant appearance in text: VWF: 1378C>T
PubMed Link: 34237177
Variant Present in the following documents:
  • JCLA-35-e23896.pdf
View BVdb publication page