Allele Registry

Canonical Allele Identifier: PA2826066462

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000119001

ClinVar Variation:

132118

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Gly143Arg	CA345600 NM_001172478.2:c.427G>A CA371590379 NM_001172478.2:c.427G>C