Allele Registry

Canonical Allele Identifier: PA2826066473

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000119004

ClinVar Variation:

132121

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Arg159Lys	CA345607 NM_001172478.2:c.476G>A