Allele Registry

Canonical Allele Identifier: PA278599

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000023387

RCV000119003

ClinVar Variation:

30434

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Phe274Leu	CA278595 NM_001172477.1:c.822T>A CA371590274 NM_001172477.1:c.822T>G CA371590284 NM_001172477.1:c.820T>C