VWF c.1906_1908delinsTGT ;(p.R636C)

Variant ID: 12-6166060-TCT-ACA

NM_000552.3(VWF):c.1906_1908delinsTGT;(p.R636C)

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:

Molecular insight into human platelet antigens: structural and evolutionary conservation analyses offer new perspective to immunogenic disorders.

Transfusion
Landau, Meytal M; Rosenberg, Nurit N
Publication Date: 2011-03

Variant appearance in text: VWF: Arg636Cys
PubMed Link: 20804530
Variant Present in the following documents:
  • Main text
  • trf0051-0558.pdf
View BVdb publication page