Allele Registry

Canonical Allele Identifier: PA2826066510

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000119012

ClinVar Variation:

132125

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Leu265Val	CA345618 NM_001172478.2:c.793T>G