Allele Registry

Canonical Allele Identifier: PA180568

Gene: EGFR HGNC NCBI

ClinVar Allele:

174243

ClinVar RCV:

RCV000154231

RCV003998241

ClinVar Variation:

177647

HGVS (amino-acid)	Matching Registered Transcripts
NP_005219.2:p.Leu747_Ser752del	CA180566 NM_005228.5:c.2239_2256del CA645561520 NM_005228.5:c.2238_2255delinsGCAACA CA645561521 NM_005228.5:c.2238_2256delinsGCAA CA645561524 NM_005228.5:c.2239_2256delinsCAA CA645561528 NM_005228.5:c.2239_2255delinsCAACA CA2573129747 NM_005228.5:c.2239_2255delinsCCACA