Canonical Allele Identifier: PA271460
Gene: EBP HGNC NCBI

Linked Data

ClinVar Variation Id: 158539
ClinVar RCV Id: RCV000145931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006570.1:p.Trp101Cys
CA271459
NM_006579.3:c.303G>T
CA412852050
NM_006579.3:c.303G>C