Canonical Allele Identifier: PA645474105
Gene: EPOR HGNC NCBI

Linked Data

ClinVar Variation Id: 328149
ClinVar RCV Id: RCV000283000
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000112.1:p.Leu199Pro
CA9210692
NM_000121.4:c.596T>C