Canonical Allele Identifier: PA110453
Gene: EBP HGNC NCBI

Linked Data

ClinVar Variation Id: 11492
ClinVar RCV Id: RCV000012247 RCV003329229
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Amino-acid Alleles

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