Allele Registry

Canonical Allele Identifier: PA112756

Gene: EIF2B5 HGNC NCBI

ClinVar RCV:

RCV002664327

ClinVar Variation:

2203468

HGVS (amino-acid)	Matching Registered Transcripts
NP_003898.2:p.Val73Gly	CA88840226 NM_003907.3:c.218T>G