Allele Registry

Canonical Allele Identifier: PA345569

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000118987

RCV002514588

ClinVar Variation:

132108

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Asp70Asn	CA345565 NM_015713.5:c.208G>A