Allele Registry

Canonical Allele Identifier: PA915992710

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000118995

RCV001753498

ClinVar Variation:

132113

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Phe71Ser	CA345576 NM_001172478.2:c.212T>C