Allele Registry

Canonical Allele Identifier: PA321321

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000196901

ClinVar Variation:

215100

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Asp142Tyr	CA321318 NM_001172477.1:c.424G>T