Allele Registry

Canonical Allele Identifier: PA345589

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000118997

RCV000505928

ClinVar Variation:

132115

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Thr144Ile	CA345586 NM_015713.5:c.431C>T