Canonical Allele Identifier: PA1139768705
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 16609
ClinVar RCV Id: RCV000018083 RCV000018084 RCV000150629 RCV000211323 RCV000418019 RCV000435684 RCV000987885
ClinVar Variation Id: 376280
ClinVar RCV Id: RCV000435887
ClinVar Variation Id: 376282
ClinVar RCV Id: RCV000425876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333827.1:p.Leu858Arg
CA126713
NM_001346898.1:c.2573T>G
CA16602728
NM_001346898.1:c.2572_2573delinsAG
CA16602730
NM_001346898.1:c.2573_2574delinsGT
CA645561613
NM_001346898.1:c.2573_2574delinsGA