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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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