Canonical Allele Identifier: PA645397591
Gene: EBP HGNC NCBI

Linked Data

ClinVar Variation Id: 209040
ClinVar RCV Id: RCV000190983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006570.1:p.Trp47Arg
CA10575772
NM_006579.3:c.139T>C
CA412851300
NM_006579.3:c.139T>A