Canonical Allele Identifier: PA645397612
Gene: EBP HGNC NCBI

Linked Data

ClinVar Variation Id: 265110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006570.1:p.Arg147Cys
CA10588787
NM_006579.3:c.439C>T