Allele Registry

Canonical Allele Identifier: PA135796

Gene: EGFR HGNC NCBI

ClinVar Variation Id: 45233

ClinVar RCV Id: RCV000038389

ClinVar Variation Id: 163343

ClinVar Variation Id: 177620

HGVS (amino-acid)	Matching Registered Transcripts
NP_005219.2:p.Glu746_Ala750del	CA135794 NM_005228.5:c.2232_2249delinsAAA CA175996 NM_005228.5:c.2235_2249del CA175997 NM_005228.5:c.2237_2248delinsCCC CA180531 NM_005228.5:c.2236_2250del CA180619 NM_005228.5:c.2235_2248delinsAATTC CA180653 NM_005228.5:c.2237_2248delinsCAC CA645561497 NM_005228.5:c.2236_2248delinsCAAC CA645561513 NM_005228.5:c.2237_2250delinsTCCCT CA645561522 NM_005228.5:c.2238_2248delinsTC