KIT c.229A>C ;(p.N77H)

Variant ID: 4-55561839-A-C

NM_000222.2(KIT):c.229A>C;(p.N77H)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic heterogeneity in hepatocellular carcinoma and paired bone metastasis revealed by next-generation sequencing.

International Journal Of Clinical And Experimental Pathology
Jin, Ketao K; Lan, Huanrong H; Wang, Xuanwei X; Lv, Jieqing J
Publication Date: 2017

Variant appearance in text: KIT: 229A>C; Asn77His
PubMed Link: 31966388
Variant Present in the following documents:
  • Main text
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