Allele Registry

Canonical Allele Identifier: PA112739

Gene: EIF2B5 HGNC NCBI

ClinVar RCV:

RCV003221409

ClinVar Variation:

5943

HGVS (amino-acid)	Matching Registered Transcripts
NP_003898.2:p.Trp628Arg	CA340474 NM_003907.3:c.1882T>C CA355393978 NM_003907.3:c.1882T>A