Canonical Allele Identifier: PA181004
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 177920
ClinVar RCV Id: RCV000154579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Glu746_Thr751delinsIle
CA180803
NM_005228.5:c.2235_2251delinsAATTC
CA181002
NM_005228.5:c.2236_2252delinsAT
CA645561490
NM_005228.5:c.2235_2252delinsAAT
CA645561498
NM_005228.5:c.2236_2253delinsATTCCT