Allele Registry

Canonical Allele Identifier: PA321322

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000196901

ClinVar Variation:

215100

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Asp70Tyr	CA321318 NM_015713.5:c.208G>T