Allele Registry

Canonical Allele Identifier: PA2827387984

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000154579

ClinVar Variation:

177920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333826.1:p.Glu701_Thr706delinsIle	CA180803 NM_001346897.1:c.2100_2116delinsAATTC CA181002 NM_001346897.1:c.2101_2117delinsAT CA645561490 NM_001346897.1:c.2100_2117delinsAAT CA645561498 NM_001346897.1:c.2101_2118delinsATTCCT CA2850447143 NM_001346897.1:c.2100_2118delinsAATT