Allele Registry

Canonical Allele Identifier: PA2827393330

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000154579

ClinVar Variation:

177920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333829.1:p.Glu693_Thr698delinsIle	CA180803 NM_001346900.1:c.2076_2092delinsAATTC CA181002 NM_001346900.1:c.2077_2093delinsAT CA645561490 NM_001346900.1:c.2076_2093delinsAAT CA645561498 NM_001346900.1:c.2077_2094delinsATTCCT CA2850447143 NM_001346900.1:c.2076_2094delinsAATT