Allele Registry

Canonical Allele Identifier: PA099091

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000119000

ClinVar Variation:

132117

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Glu194Gly	CA345596 NM_015713.5:c.581A>G