Canonical Allele Identifier: PA112557
Gene: EIF2B5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1479566
ClinVar RCV Id: RCV001990979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003898.2:p.Arg269Gly
CA88840902
NM_003907.3:c.805C>G