Canonical Allele Identifier: PA135939
Gene: EGFR HGNC NCBI
ClinVar RCV:
RCV000038442
ClinVar Variation:
45286
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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