Allele Registry

Canonical Allele Identifier: PA279003

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000198969

ClinVar Variation:

216993

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Gly212_Leu213insSer	CA279000 NM_015713.5:c.635_636insAAG