Allele Registry

Canonical Allele Identifier: PA2826066466

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000023387

RCV000119003

ClinVar Variation:

30434

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Phe150Leu	CA278595 NM_001172478.2:c.450T>A CA371590274 NM_001172478.2:c.450T>G CA371590284 NM_001172478.2:c.448T>C