Allele Registry

Canonical Allele Identifier: PA2826066463

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000196346

ClinVar Variation:

215092

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Gly148Glu	CA320760 NM_001172478.2:c.443G>A