Allele Registry

Canonical Allele Identifier: PA2827387999

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000154236

RCV003998242

ClinVar Variation:

177649

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333826.1:p.Leu702_Thr706del	CA126716 NM_001346897.1:c.2104_2116delinsC CA180569 NM_001346897.1:c.2105_2119del CA180573 NM_001346897.1:c.2103_2116delinsGC CA158932632 NM_001346897.1:c.2105_2116del CA645561518 NM_001346897.1:c.2103_2117delinsGCA CA645561527 NM_001346897.1:c.2104_2118delinsAAT CA645561530 NM_001346897.1:c.2104_2117delinsCA