Canonical Allele Identifier: PA126721
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 16611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Gly719Cys
CA126719
NM_005228.5:c.2155G>T
CA645550316
NM_005228.5:c.2154_2155delinsTT