Allele Registry

Canonical Allele Identifier: PA345590

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000118997

RCV000505928

ClinVar Variation:

132115

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Thr216Ile	CA345586 NM_001172477.1:c.647C>T