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RET c.*1046G>A
Variant ID: 10-43624763-G-A
NM_020975.4(
RET
):c.*1046G>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:
RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.
Plos One
Vaclavikova, Eliska E; Dvorakova, Sarka S; Skaba, Richard R; Pos, Lucie L; Sykorova, Vlasta V; Halkova, Tereza T; Vcelak, Josef J; Bendlova, Bela B
Publication Date: 2014
Variant appearance in text: rs143948954
PubMed Link:
24897126
Variant Present in the following documents:
Main text
pone.0098957.pdf
View BVdb publication page