Allele Registry

Canonical Allele Identifier: PA345579

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000118995

RCV001753498

ClinVar Variation:

132113

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Phe123Ser	CA345576 NM_015713.5:c.368T>C