Allele Registry

Canonical Allele Identifier: PA180562

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000154229

ClinVar Variation:

177645

HGVS (amino-acid)	Matching Registered Transcripts
NP_005219.2:p.[Glu746_Glu749del;Thr751del]	CA180560 NM_005228.5:c.2237_2251del CA645561492 NM_005228.5:c.2235_2251delinsAG