Canonical Allele Identifier: PA135939
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45286
ClinVar RCV Id: RCV000038442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005219.2:p.Lys860Asn
CA135937
NM_005228.5:c.2580A>T
CA367580289
NM_005228.5:c.2580A>C