Allele Registry

Canonical Allele Identifier: PA135829

Gene: EGFR HGNC NCBI

ClinVar RCV:

RCV000038400

RCV000435465

ClinVar Variation:

45244

HGVS (amino-acid)	Matching Registered Transcripts
NP_005219.2:p.Asp761Tyr	CA135827 NM_005228.5:c.2281G>T