Allele Registry

Canonical Allele Identifier: PA112622

Gene: EIF2B5 HGNC NCBI

ClinVar RCV:

RCV000824637

RCV000853415

RCV003325978

ClinVar Variation:

666195

HGVS (amino-acid)	Matching Registered Transcripts
NP_003898.2:p.Arg339Trp	CA2726569 NM_003907.3:c.1015C>T