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PC c.139_141delinsTGT ;(p.E47C)
Variant ID: 11-66639338-CTC-ACA
NM_001040716.1(
PC
):c.139_141delinsTGT;(p.E47C)
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:
Disconnect between the developing eye and craniofacial prominences in the avian embryo.
Mechanisms Of Development
Jomaa, Jamil J; MartÃnez-Vargas, Jessica J; Essaili, Shadya S; Haider, Nida N; Abramyan, John J
Publication Date: 2020-03
Variant appearance in text: PC: E47C
PubMed Link:
32044294
Variant Present in the following documents:
Main text
View BVdb publication page