Bibliome.ai browser hg19
Search
About
Stats
FAQ
HFE c.109_110delinsTG ;(p.A37C)
Variant ID: 6-26091101-GC-TG
NM_000410.3(
HFE
):c.109_110delinsTG;(p.A37C)
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 child with hyperferritinemia: case report.
Italian Journal Of Pediatrics
Serra, Melania M; Longo, Filomena F; Roetto, Antonella A; Sandri, Alessandro A; Piga, Antonio A
Publication Date: 2011-05-12
Variant appearance in text: HFE: A37C
PubMed Link:
21569394
Variant Present in the following documents:
Main text
1824-7288-37-20.pdf
View BVdb publication page