Allele Registry

Canonical Allele Identifier: PA099081

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000005721

RCV000119007

ClinVar Variation:

5390

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Cys236Phe	CA117483 NM_015713.5:c.707G>T