Allele Registry

Canonical Allele Identifier: PA278604

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000023388

RCV000119008

RCV001582496

ClinVar Variation:

30435

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Gly345Ser	CA278600 NM_001172477.1:c.1033G>A