Allele Registry

Canonical Allele Identifier: PA2827389823

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000154236

RCV003998242

ClinVar Variation:

177649

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333827.1:p.Leu747_Thr751del	CA126716 NM_001346898.1:c.2239_2251delinsC CA180569 NM_001346898.1:c.2240_2254del CA180573 NM_001346898.1:c.2238_2251delinsGC CA158932632 NM_001346898.1:c.2240_2251del CA645561518 NM_001346898.1:c.2238_2252delinsGCA CA645561527 NM_001346898.1:c.2239_2253delinsAAT CA645561530 NM_001346898.1:c.2239_2252delinsCA