Canonical Allele Identifier: PA1139701932
Gene: EGFR HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Ala864Thr
CA367580302
NM_005228.5:c.2590G>A