Canonical Allele Identifier: PA2827387998
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 177971
ClinVar RCV Id: RCV000154644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333826.1:p.[Glu701del;Arg703_Thr706del]
CA181093
NM_001346897.1:c.2097_2117delinsAAAGTT
CA645561500
NM_001346897.1:c.2101_2117delinsCT