Allele Registry

Canonical Allele Identifier: PA2827391556

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000154239

RCV000154445

RCV003998243

ClinVar Variation:

177652

177813

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333828.1:p.Glu701_Ser707delinsVal	CA180574 NM_001346899.1:c.2102_2120delinsT CA180811 NM_001346899.1:c.2102_2121delinsTC CA645561509 NM_001346899.1:c.2102_2121delinsTG CA2573049007 NM_001346899.1:c.2100_2120delinsAGT CA2850447208 NM_001346899.1:c.2102_2121delinsTA