Canonical Allele Identifier: PA135856
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45257
ClinVar RCV Id: RCV000038413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Asp770_Asn771insGlyLeu
CA135854
NM_005228.5:c.2310_2311insGGGTTG
CA645561585
NM_005228.5:c.2310_2311insGGGTTA