Allele Registry

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Canonical Allele Identifier: PA2827395438

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_001333870.1:p.Leu591Arg	CA126713 NM_001346941.2:c.1772T>G CA16602728 NM_001346941.2:c.1771_1772delinsAG CA16602730 NM_001346941.2:c.1772_1773delinsGT CA645561613 NM_001346941.2:c.1772_1773delinsGA