Allele Registry

Canonical Allele Identifier: PA915992699

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000118991

RCV002262712

ClinVar Variation:

132112

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Arg58Cys	CA345571 NM_001172478.2:c.172C>T