Allele Registry

Canonical Allele Identifier: PA322921

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000198415

RCV001089490

ClinVar Variation:

215095

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Arg40Cys	CA322917 NM_015713.5:c.118C>T