Allele Registry

Canonical Allele Identifier: PA102520

Gene: EPOR HGNC NCBI

ClinVar Allele:

31637

ClinVar RCV:

RCV000018068

RCV000893045

RCV003321483

ClinVar Variation:

16598

HGVS (amino-acid)	Matching Registered Transcripts
NP_000112.1:p.Asn487Ser	CA126702 NM_000121.4:c.1460A>G