Allele Registry

Canonical Allele Identifier: PA2827393349

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000154236

RCV003998242

ClinVar Variation:

177649

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333829.1:p.Leu694_Thr698del	CA126716 NM_001346900.1:c.2080_2092delinsC CA180569 NM_001346900.1:c.2081_2095del CA180573 NM_001346900.1:c.2079_2092delinsGC CA158932632 NM_001346900.1:c.2081_2092del CA645561518 NM_001346900.1:c.2079_2093delinsGCA CA645561527 NM_001346900.1:c.2080_2094delinsAAT CA645561530 NM_001346900.1:c.2080_2093delinsCA