CYP21A2 c.*443T>C

Variant ID: 6-32009354-T-C

NM_000500.7(CYP21A2):c.*443T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Novel method to characterize CYP21A2 in Florida patients with congenital adrenal hyperplasia and commercially available cell lines.

Molecular Genetics And Metabolism Reports
Greene, Christopher N CN; Cordovado, Suzanne K SK; Turner, Daniel P DP; Keong, Lisa M LM; Shulman, Dorothy D; Mueller, Patricia W PW
Publication Date: 2014

Variant appearance in text: rs6457476
PubMed Link: 27896104
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page