Allele Registry

Canonical Allele Identifier: PA345611

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000119004

ClinVar Variation:

132121

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Arg283Lys	CA345607 NM_001172477.1:c.848G>A