Allele Registry

Canonical Allele Identifier: PA117486

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000005721

RCV000119007

ClinVar Variation:

5390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Cys308Phe	CA117483 NM_001172477.1:c.923G>T