Canonical Allele Identifier: PA135913
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Arg831Cys
CA135911
NM_005228.5:c.2491C>T