Allele Registry

Canonical Allele Identifier: PA324621

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV005187150

ClinVar Variation:

3717775

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Thr218Ala	CA324618 NM_015713.5:c.652A>G