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HFE c.78T>G ;(p.R26=)
Variant ID: 6-26091070-T-G
NM_000410.3(
HFE
):c.78T>G;(p.R26=)
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:
Deletion of murine Smn exon 7 directed to liver leads to severe defect of liver development associated with iron overload.
The American Journal Of Pathology
Vitte, Jérémie M JM; Davoult, Bénédicte B; Roblot, Natacha N; Mayer, Michèle M; Joshi, Vandana V; Courageot, Sabrina S; Tronche, François F; Vadrot, Jacqueline J; Moreau, Marie Helene MH; Kemeny, François F; Melki, Judith J
Publication Date: 2004-11
Variant appearance in text: HFE: R26R
PubMed Link:
15509541
Variant Present in the following documents:
Main text
View BVdb publication page