Canonical Allele Identifier: PA271481
Gene: EBP HGNC NCBI

Linked Data

ClinVar Variation Id: 158550
ClinVar RCV Id: RCV000145942
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006570.1:p.Gly161Arg
CA271480
NM_006579.3:c.481G>A
CA412852740
NM_006579.3:c.481G>C