ACVRL1 c.1047_1048insT ;(p.G350Wfs*42)

Variant ID: 12-52309283-G-GT

NM_000020.2(ACVRL1):c.1047_1048insT;(p.G350Wfs*42)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease.

Journal Of Medical Genetics
Abdalla, S A SA; Letarte, M M
Publication Date: 2006-02

Variant appearance in text: N/A
PubMed Link: 15879500
Variant Present in the following documents:
View BVdb publication page