Allele Registry

Canonical Allele Identifier: PA2827395192

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000154579

ClinVar Variation:

177920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333870.1:p.Glu479_Thr484delinsIle	CA180803 NM_001346941.2:c.1434_1450delinsAATTC CA181002 NM_001346941.2:c.1435_1451delinsAT CA645561490 NM_001346941.2:c.1434_1451delinsAAT CA645561498 NM_001346941.2:c.1435_1452delinsATTCCT CA2850447143 NM_001346941.2:c.1434_1452delinsAATT