Canonical Allele Identifier: PA2827388018
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333826.1:p.Ala705Pro
CA135812
NM_001346897.1:c.2113G>C