Allele Registry

Canonical Allele Identifier: PA279004

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000198969

ClinVar Variation:

216993

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Gly284_Leu285insSer	CA279000 NM_001172477.1:c.851_852insAAG