Allele Registry

Canonical Allele Identifier: PA2827391099

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000423834

ClinVar Variation:

376341

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333828.1:p.Ser447Arg	CA16602784 NM_001346899.1:c.1341C>A CA367579689 NM_001346899.1:c.1339A>C CA367579693 NM_001346899.1:c.1341C>G