Allele Registry

Canonical Allele Identifier: PA345564

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000118986

ClinVar Variation:

132107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Trp136Arg	CA345561 NM_001172477.1:c.406T>C CA371595835 NM_001172477.1:c.406T>A