Allele Registry

Canonical Allele Identifier: PA117500

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000005724

RCV000118992

RCV001596931

RCV003147275

ClinVar Variation:

5393

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Arg182His	CA117497 NM_001172477.1:c.545G>A