Allele Registry

Canonical Allele Identifier: PA112557

Gene: EIF2B5 HGNC NCBI

ClinVar RCV:

RCV001990979

ClinVar Variation:

1479566

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