Canonical Allele Identifier: PA915957704
Gene: EPOR HGNC NCBI

Linked Data

ClinVar Variation Id: 713659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000112.1:p.Ala99Val
CA9210805
NM_000121.4:c.296C>T