Allele Registry

Canonical Allele Identifier: PA2826066474

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000198969

ClinVar Variation:

216993

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Gly160_Leu161insSer	CA279000 NM_001172478.2:c.479_480insAAG