Allele Registry

Canonical Allele Identifier: PA345580

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000118995

RCV001753498

ClinVar Variation:

132113

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Phe195Ser	CA345576 NM_001172477.1:c.584T>C