Allele Registry

Canonical Allele Identifier: PA110453

Gene: EBP HGNC NCBI

ClinVar RCV:

RCV000012247

RCV003329229

ClinVar Variation:

11492

HGVS (amino-acid)	Matching Registered Transcripts
NP_006570.1:p.Arg147His	CA255907 NM_006579.3:c.440G>A