VWF c.323G>A ;(p.R108K)

Variant ID: 12-6220032-C-T

NM_000552.3(VWF):c.323G>A;(p.R108K)

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:

Morbidities and mortality in patients with hereditary thrombotic thrombocytopenic purpura.

Blood Advances
Borogovac, Azra A; Reese, Jessica A JA; Gupta, Samiksha S; George, James N JN
Publication Date: 2022-02-08

Variant appearance in text: VWF: 323G>A
PubMed Link: 34807988
Variant Present in the following documents:
  • advancesADV2021005760-suppl1.pdf
View BVdb publication page