Canonical Allele Identifier: PA126715
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 16609
ClinVar Variation Id: 376280
ClinVar RCV Id: RCV000435887
ClinVar Variation Id: 376282
ClinVar RCV Id: RCV000425876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Leu858Arg
CA126713
NM_005228.5:c.2573T>G
CA16602728
NM_005228.5:c.2572_2573delinsAG
CA16602730
NM_005228.5:c.2573_2574delinsGT
CA645561613
NM_005228.5:c.2573_2574delinsGA