Allele Registry

Canonical Allele Identifier: PA915992714

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000118997

RCV000505928

ClinVar Variation:

132115

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Thr92Ile	CA345586 NM_001172478.2:c.275C>T