Canonical Allele Identifier: PA2573088813
Gene: EBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1302551
ClinVar RCV Id: RCV001756225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006570.1:p.Met121Val
CA412852331
NM_006579.3:c.361A>G