Allele Registry

Canonical Allele Identifier: PA2827026369

Gene: EIF2B4 HGNC NCBI

ClinVar RCV:

RCV003221398

ClinVar Variation:

4122

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305897.1:p.Tyr294His	CA116653 NM_001318968.2:c.880T>C