Canonical Allele Identifier: PA1139716339
Gene: EBP HGNC NCBI

Linked Data

ClinVar Variation Id: 988320
ClinVar RCV Id: RCV001269598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006570.1:p.Gly157Ser
CA412852676
NM_006579.3:c.469G>A