Canonical Allele Identifier: PA2741929456
Gene: EBP HGNC NCBI

Linked Data

ClinVar Variation Id: 2765456
ClinVar RCV Id: RCV003578325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006570.1:p.Tyr111Asn
CA412852174
NM_006579.3:c.331T>A