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EGF c.968G>T ;(p.G323V)
Variant ID: 4-110880495-G-T
NM_001963.4(
EGF
):c.968G>T;(p.G323V)
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:
The molecular basis of ferroportin-linked hemochromatosis.
Proceedings Of The National Academy Of Sciences Of The United States Of America
De Domenico, Ivana I; Ward, Diane McVey DM; Nemeth, Elizabeta E; Vaughn, Michael B MB; Musci, Giovanni G; Ganz, Tomas T; Kaplan, Jerry J
Publication Date: 2005-06-21
Variant appearance in text: EGF: G323V
PubMed Link:
15956209
Variant Present in the following documents:
Main text
View BVdb publication page