Allele Registry

Canonical Allele Identifier: PA2826066459

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000119000

ClinVar Variation:

132117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Glu142Gly	CA345596 NM_001172478.2:c.425A>G