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F13A1 c.320-2256C>A
Variant ID: 6-6269298-G-T
NM_000129.3(
F13A1
):c.320-2256C>A
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:
How to Assess Founder Effect in Patients with Congenital Factor XIII Deficiency.
International Journal Of Hematology-Oncology And Stem Cell Research
Shahraki, Hojat H; Dorgalaleh, Akbar A; Fathi, Majid M; Tabibian, Shadi S; Teimourian, Shahram S; Mollanoori, Hasan H; Khiabani, Alireza A; Zaker, Farhad F
Publication Date: 2020-10-01
Variant appearance in text: rs4960181
PubMed Link:
33603988
Variant Present in the following documents:
Main text
IJHOSCR-14-265.pdf
View BVdb publication page