Canonical Allele Identifier: PA135820
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45241
ClinVar RCV Id: RCV000038397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Lys754Glu
CA135818
NM_005228.5:c.2260A>G