Allele Registry

Canonical Allele Identifier: PA2826194200

Gene: EIF4G1 HGNC NCBI

ClinVar RCV:

RCV001529161

ClinVar Variation:

1174883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001181875.2:p.Thr168Ala	CA2731921 NM_001194946.2:c.502A>G