Canonical Allele Identifier: PA135942
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Leu861Arg
CA135940
NM_005228.5:c.2582T>G