Allele Registry

Canonical Allele Identifier: PA117504

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000005725

RCV000118994

ClinVar Variation:

5394

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Arg193His	CA117501 NM_001172477.1:c.578G>A