Allele Registry

Canonical Allele Identifier: PA2826066406

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000196901

ClinVar Variation:

215100

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Asp18Tyr	CA321318 NM_001172478.2:c.52G>T