Allele Registry

Canonical Allele Identifier: PA110463

Gene: EBP HGNC NCBI

ClinVar RCV:

RCV000012240

RCV002276542

RCV002512979

ClinVar Variation:

11485

HGVS (amino-acid)	Matching Registered Transcripts
NP_006570.1:p.Glu80Lys	CA255900 NM_006579.3:c.238G>A