Allele Registry

Canonical Allele Identifier: PA2827395197

Gene: EGFR HGNC NCBI

ClinVar Allele:

174245

ClinVar RCV:

RCV000154236

RCV003998242

ClinVar Variation:

177649

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333870.1:p.Leu480_Thr484del	CA126716 NM_001346941.2:c.1438_1450delinsC CA180569 NM_001346941.2:c.1439_1453del CA180573 NM_001346941.2:c.1437_1450delinsGC CA158932632 NM_001346941.2:c.1439_1450del CA645561518 NM_001346941.2:c.1437_1451delinsGCA CA645561527 NM_001346941.2:c.1438_1452delinsAAT CA645561530 NM_001346941.2:c.1438_1451delinsCA