Canonical Allele Identifier: PA135829
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45244
ClinVar RCV Id: RCV000038400 RCV000435465
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Asp761Tyr
CA135827
NM_005228.5:c.2281G>T