PC c.3122G>C ;(p.G1041A)

Variant ID: 11-66617107-C-G

NM_001040716.1(PC):c.3122G>C;(p.G1041A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutation analysis of the ATP7B gene and genotype-phenotype correlation in Chinese patients with Wilson disease.

Bmc Gastroenterology
Li, Mingming M; Ma, Jing J; Wang, Wenlong W; Yang, Xu X; Luo, Kaizhong K
Publication Date: 2021-09-01

Variant appearance in text: PC: 3122G>C
PubMed Link: 34470610
Variant Present in the following documents:
  • 12876_2021_Article_1911.pdf
View BVdb publication page