Allele Registry

Canonical Allele Identifier: PA117482

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000005719

RCV000118999

ClinVar Variation:

5388

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Glu266Lys	CA117479 NM_001172477.1:c.796G>A