EGFR c.1688T>C ;(p.L563P)

Variant ID: 7-55231482-T-C

NM_005228.3(EGFR):c.1688T>C;(p.L563P)

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:

Nonsyndromic Split-Hand/Foot Malformation: Recent Classification.

Molecular Syndromology
Umair, Muhammad M; Hayat, Amir A
Publication Date: 2020-01

Variant appearance in text: EGFR: Leu563Pro
PubMed Link: 32021595
Variant Present in the following documents:
  • Main text
View BVdb publication page