Canonical Allele Identifier: PA135823
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45242
ClinVar RCV Id: RCV000038398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Lys757Met
CA135821
NM_005228.5:c.2270A>T