Allele Registry

Canonical Allele Identifier: PA345599

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000119000

ClinVar Variation:

132117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Glu266Gly	CA345596 NM_001172477.1:c.797A>G