Canonical Allele Identifier: PA093397
Gene: EIF2B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4121
ClinVar RCV Id: RCV003221397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001029288.1:p.Cys465Arg
CA116652
NM_001034116.2:c.1393T>C