Allele Registry

Canonical Allele Identifier: PA2827026229

Gene: EIF2B4 HGNC NCBI

ClinVar RCV:

RCV003448660

ClinVar Variation:

2671575

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305896.1:p.Arg452Trp	CA44509202 NM_001318967.2:c.1354C>T