Allele Registry

Canonical Allele Identifier: PA322920

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000198415

RCV001089490

ClinVar Variation:

215095

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Arg112Cys	CA322917 NM_001172477.1:c.334C>T