Allele Registry

Canonical Allele Identifier: PA345621

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000119012

ClinVar Variation:

132125

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Leu389Val	CA345618 NM_001172477.1:c.1165T>G