Canonical Allele Identifier: PA204967
Gene: EBP HGNC NCBI

Linked Data

ClinVar Variation Id: 209039
ClinVar RCV Id: RCV000190982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006570.1:p.Ile75Asn
CA204966
NM_006579.3:c.224T>A