PKD1 c.6695T>C ;(p.F2232S)

Variant ID: 16-2158473-A-G

NM_001009944.2(PKD1):c.6695T>C;(p.F2232S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Analysis of mutations in six Chinese families with autosomal dominant polycystic kidney disease.

American Journal Of Translational Research
Wang, Hanlu H; Dai, Sen S; Zhang, Jianhui J; Li, Yi Y; Gan, Yumian Y; Lu, Tao T; Zhu, Yaobin Y; Wu, Jiabin J; Lin, Ning N; Tang, Faqiang F; Luo, Jiewei J
Publication Date: 2020

Variant appearance in text: PKD1: 6695T>C; Phe2232Ser
PubMed Link: 33437386
Variant Present in the following documents:
  • Main text
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