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CP c.691_693del ;(p.Y231del)
Variant ID: 3-148927086-GGTA-G
NM_000096.3(
CP
):c.691_693del;(p.Y231del)
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:
A 10-year Follow-up Study of a Japanese Family with Ferroportin Disease A: Mild Iron Overload with Mild Hyperferritinemia Co-occurring with Hyperhepcidinemia May Be Benign.
Internal Medicine (Tokyo, Japan)
Hayashi, Hisao H; Yano, Motoyoshi M; Urawa, Naohito N; Mizutani, Akane A; Hamaoka, Shima S; Araki, Jun J; Kojima, Yuji Y; Naito, Yutaka Y; Kato, Ayako A; Tatsumi, Yasuaki Y; Kato, Koichi K
Publication Date: 2018-10-01
Variant appearance in text: CP: Y231del
PubMed Link:
29780118
Variant Present in the following documents:
Main text
View BVdb publication page