Allele Registry

Canonical Allele Identifier: PA2827389818

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000154579

ClinVar Variation:

177920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333827.1:p.Glu746_Thr751delinsIle	CA180803 NM_001346898.1:c.2235_2251delinsAATTC CA181002 NM_001346898.1:c.2236_2252delinsAT CA645561490 NM_001346898.1:c.2235_2252delinsAAT CA645561498 NM_001346898.1:c.2236_2253delinsATTCCT CA2850447143 NM_001346898.1:c.2235_2253delinsAATT