This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA913194859
Gene: EBP HGNC NCBI
ClinVar RCV:
RCV000762632
ClinVar Variation:
624410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006570.1:p.Asp93Gly
CA412851864
NM_006579.3:c.278A>G